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Dates: 1995 – 1999

You searched for subject:(Chromosome). Showing records 1 – 30 of 54 total matches.

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1. Zhong, X.B. Tomato genome mapping by fluorescence in situ hybridisation = Kartering van het tomatengenoom met behulp van fluorescentie in situ hybridisatie.

Degree: 1998, Agricultural University

  The general introduction reviews the progress in tomato genome mapping using classical genetics, cytogenetics, and molecular genetics, emphasising the great potential of fluorescence in… (more)

Subjects/Keywords: moleculaire biologie; genetische code; methodologie; technieken; chromosoomkaarten; genkartering; somatische hybridisatie; verwijderde hybridisatie; solanum lycopersicum; tomaten; Moleculaire plantenbiologie; molecular biology; genetic code; methodology; techniques; chromosome maps; gene mapping; somatic hybridization; wide hybridization; solanum lycopersicum; tomatoes; Plant Molecular Biology

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APA (6th Edition):

Zhong, X. B. (1998). Tomato genome mapping by fluorescence in situ hybridisation = Kartering van het tomatengenoom met behulp van fluorescentie in situ hybridisatie. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/40625 ; urn:nbn:nl:ui:32-40625 ; urn:nbn:nl:ui:32-40625 ; http://library.wur.nl/WebQuery/wurpubs/40625

Chicago Manual of Style (16th Edition):

Zhong, X B. “Tomato genome mapping by fluorescence in situ hybridisation = Kartering van het tomatengenoom met behulp van fluorescentie in situ hybridisatie.” 1998. Doctoral Dissertation, Agricultural University. Accessed December 14, 2019. http://library.wur.nl/WebQuery/wurpubs/40625 ; urn:nbn:nl:ui:32-40625 ; urn:nbn:nl:ui:32-40625 ; http://library.wur.nl/WebQuery/wurpubs/40625.

MLA Handbook (7th Edition):

Zhong, X B. “Tomato genome mapping by fluorescence in situ hybridisation = Kartering van het tomatengenoom met behulp van fluorescentie in situ hybridisatie.” 1998. Web. 14 Dec 2019.

Vancouver:

Zhong XB. Tomato genome mapping by fluorescence in situ hybridisation = Kartering van het tomatengenoom met behulp van fluorescentie in situ hybridisatie. [Internet] [Doctoral dissertation]. Agricultural University; 1998. [cited 2019 Dec 14]. Available from: http://library.wur.nl/WebQuery/wurpubs/40625 ; urn:nbn:nl:ui:32-40625 ; urn:nbn:nl:ui:32-40625 ; http://library.wur.nl/WebQuery/wurpubs/40625.

Council of Science Editors:

Zhong XB. Tomato genome mapping by fluorescence in situ hybridisation = Kartering van het tomatengenoom met behulp van fluorescentie in situ hybridisatie. [Doctoral Dissertation]. Agricultural University; 1998. Available from: http://library.wur.nl/WebQuery/wurpubs/40625 ; urn:nbn:nl:ui:32-40625 ; urn:nbn:nl:ui:32-40625 ; http://library.wur.nl/WebQuery/wurpubs/40625

2. Peters, A.H.F.M. Non-homologous chromosome synapsis during mouse meiosis : consequences for male fertility and survival of progeny.

Degree: 1997, Agricultural University

 In the mouse, heterozygosity for several reciprocal and Robertsonian translocations is associated with impairment of chromosome synapsis and suppression of crossover formation in segments near… (more)

Subjects/Keywords: muridae; muizen; meiose; geslachtelijke voortplanting; parthenogenese; polyembryologie; vruchtbaarheid; overleving; levensvatbaarheid; interacties; milieu; uitsterven; stofverplaatsing; chromosoomtranslocatie; chromosomen; cytologie; histologie; Genetica (algemeen); Voortplanting en vruchtbaarheid; muridae; mice; meiosis; sexual reproduction; parthenogenesis; polyembryony; fertility; survival; viability; interactions; environment; extinction; translocation; chromosome translocation; chromosomes; cytology; histology; Genetics (General); Reproduction and Fertility

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APA (6th Edition):

Peters, A. H. F. M. (1997). Non-homologous chromosome synapsis during mouse meiosis : consequences for male fertility and survival of progeny. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/38093 ; urn:nbn:nl:ui:32-38093 ; urn:nbn:nl:ui:32-38093 ; http://library.wur.nl/WebQuery/wurpubs/38093

Chicago Manual of Style (16th Edition):

Peters, A H F M. “Non-homologous chromosome synapsis during mouse meiosis : consequences for male fertility and survival of progeny.” 1997. Doctoral Dissertation, Agricultural University. Accessed December 14, 2019. http://library.wur.nl/WebQuery/wurpubs/38093 ; urn:nbn:nl:ui:32-38093 ; urn:nbn:nl:ui:32-38093 ; http://library.wur.nl/WebQuery/wurpubs/38093.

MLA Handbook (7th Edition):

Peters, A H F M. “Non-homologous chromosome synapsis during mouse meiosis : consequences for male fertility and survival of progeny.” 1997. Web. 14 Dec 2019.

Vancouver:

Peters AHFM. Non-homologous chromosome synapsis during mouse meiosis : consequences for male fertility and survival of progeny. [Internet] [Doctoral dissertation]. Agricultural University; 1997. [cited 2019 Dec 14]. Available from: http://library.wur.nl/WebQuery/wurpubs/38093 ; urn:nbn:nl:ui:32-38093 ; urn:nbn:nl:ui:32-38093 ; http://library.wur.nl/WebQuery/wurpubs/38093.

Council of Science Editors:

Peters AHFM. Non-homologous chromosome synapsis during mouse meiosis : consequences for male fertility and survival of progeny. [Doctoral Dissertation]. Agricultural University; 1997. Available from: http://library.wur.nl/WebQuery/wurpubs/38093 ; urn:nbn:nl:ui:32-38093 ; urn:nbn:nl:ui:32-38093 ; http://library.wur.nl/WebQuery/wurpubs/38093

3. Haymes, K.M. Molecular genetic studies in Fragaria species : agrobacterium-mediated transformation and fine mapping of the Phytophthora fragariae resistance gene Rpfl.

Degree: 1997, Agricultural University

  The fungus Phytophthora fragariae, is able to cause red stele root rot in the strawberry. Symptoms of the disease is discolouration of the stele… (more)

Subjects/Keywords: plantenveredeling; ziekteresistentie; plaagresistentie; fragaria; aardbeien; plantenziekteverwekkende schimmels; phytophthora; genetische modificatie; recombinant dna; chromosoomkaarten; genkartering; Resistentieveredeling; Plantencelbiologie; Moleculaire plantenbiologie; plant breeding; disease resistance; pest resistance; fragaria; strawberries; plant pathogenic fungi; phytophthora; genetic engineering; recombinant dna; chromosome maps; gene mapping; Resistance Breeding; Plant Cell Biology; Plant Molecular Biology

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APA (6th Edition):

Haymes, K. M. (1997). Molecular genetic studies in Fragaria species : agrobacterium-mediated transformation and fine mapping of the Phytophthora fragariae resistance gene Rpfl. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/38079 ; urn:nbn:nl:ui:32-38079 ; urn:nbn:nl:ui:32-38079 ; http://library.wur.nl/WebQuery/wurpubs/38079

Chicago Manual of Style (16th Edition):

Haymes, K M. “Molecular genetic studies in Fragaria species : agrobacterium-mediated transformation and fine mapping of the Phytophthora fragariae resistance gene Rpfl.” 1997. Doctoral Dissertation, Agricultural University. Accessed December 14, 2019. http://library.wur.nl/WebQuery/wurpubs/38079 ; urn:nbn:nl:ui:32-38079 ; urn:nbn:nl:ui:32-38079 ; http://library.wur.nl/WebQuery/wurpubs/38079.

MLA Handbook (7th Edition):

Haymes, K M. “Molecular genetic studies in Fragaria species : agrobacterium-mediated transformation and fine mapping of the Phytophthora fragariae resistance gene Rpfl.” 1997. Web. 14 Dec 2019.

Vancouver:

Haymes KM. Molecular genetic studies in Fragaria species : agrobacterium-mediated transformation and fine mapping of the Phytophthora fragariae resistance gene Rpfl. [Internet] [Doctoral dissertation]. Agricultural University; 1997. [cited 2019 Dec 14]. Available from: http://library.wur.nl/WebQuery/wurpubs/38079 ; urn:nbn:nl:ui:32-38079 ; urn:nbn:nl:ui:32-38079 ; http://library.wur.nl/WebQuery/wurpubs/38079.

Council of Science Editors:

Haymes KM. Molecular genetic studies in Fragaria species : agrobacterium-mediated transformation and fine mapping of the Phytophthora fragariae resistance gene Rpfl. [Doctoral Dissertation]. Agricultural University; 1997. Available from: http://library.wur.nl/WebQuery/wurpubs/38079 ; urn:nbn:nl:ui:32-38079 ; urn:nbn:nl:ui:32-38079 ; http://library.wur.nl/WebQuery/wurpubs/38079

4. Kreike, C.M. Mapping and characterisation of quantitative trait loci conferring nematode resistance in Solanum spegazzinii.

Degree: 1995, Agricultural University

  This thesis describes the mapping and characterisation of QTLs, in Solanum spegazzinii, that are involved in resistance to the potato cyst-nematodes Globodera rostochiensis and… (more)

Subjects/Keywords: solanum tuberosum; aardappelen; plantenplagen; pratylenchus; heteroderidae; tylenchidae; chromosoomkaarten; genkartering; genetische modificatie; recombinant dna; plantenveredeling; ziekteresistentie; plaagresistentie; planten; globodera; solanum tuberosum; potatoes; plant pests; pratylenchus; heteroderidae; tylenchidae; chromosome maps; gene mapping; genetic engineering; recombinant dna; plant breeding; disease resistance; pest resistance; plants; globodera

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APA (6th Edition):

Kreike, C. M. (1995). Mapping and characterisation of quantitative trait loci conferring nematode resistance in Solanum spegazzinii. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/31220 ; urn:nbn:nl:ui:32-31220 ; urn:nbn:nl:ui:32-31220 ; http://library.wur.nl/WebQuery/wurpubs/31220

Chicago Manual of Style (16th Edition):

Kreike, C M. “Mapping and characterisation of quantitative trait loci conferring nematode resistance in Solanum spegazzinii.” 1995. Doctoral Dissertation, Agricultural University. Accessed December 14, 2019. http://library.wur.nl/WebQuery/wurpubs/31220 ; urn:nbn:nl:ui:32-31220 ; urn:nbn:nl:ui:32-31220 ; http://library.wur.nl/WebQuery/wurpubs/31220.

MLA Handbook (7th Edition):

Kreike, C M. “Mapping and characterisation of quantitative trait loci conferring nematode resistance in Solanum spegazzinii.” 1995. Web. 14 Dec 2019.

Vancouver:

Kreike CM. Mapping and characterisation of quantitative trait loci conferring nematode resistance in Solanum spegazzinii. [Internet] [Doctoral dissertation]. Agricultural University; 1995. [cited 2019 Dec 14]. Available from: http://library.wur.nl/WebQuery/wurpubs/31220 ; urn:nbn:nl:ui:32-31220 ; urn:nbn:nl:ui:32-31220 ; http://library.wur.nl/WebQuery/wurpubs/31220.

Council of Science Editors:

Kreike CM. Mapping and characterisation of quantitative trait loci conferring nematode resistance in Solanum spegazzinii. [Doctoral Dissertation]. Agricultural University; 1995. Available from: http://library.wur.nl/WebQuery/wurpubs/31220 ; urn:nbn:nl:ui:32-31220 ; urn:nbn:nl:ui:32-31220 ; http://library.wur.nl/WebQuery/wurpubs/31220

5. Beek, van der, S. The use of genetic markers in poultry breeding.

Degree: 1996, Agricultural University

  This thesis focuses on the design of linkage and quantitative trait locus (QTL) mapping experiments and on the use of genetic markers in poultry… (more)

Subjects/Keywords: genetica; heritability; genetische variatie; pluimvee; kippen; chromosoomkaarten; genkartering; moleculaire biologie; genetics; heritability; genetic variation; poultry; fowls; chromosome maps; gene mapping; molecular biology

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APA (6th Edition):

Beek, van der, S. (1996). The use of genetic markers in poultry breeding. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/33158 ; urn:nbn:nl:ui:32-33158 ; urn:nbn:nl:ui:32-33158 ; http://library.wur.nl/WebQuery/wurpubs/33158

Chicago Manual of Style (16th Edition):

Beek, van der, S. “The use of genetic markers in poultry breeding.” 1996. Doctoral Dissertation, Agricultural University. Accessed December 14, 2019. http://library.wur.nl/WebQuery/wurpubs/33158 ; urn:nbn:nl:ui:32-33158 ; urn:nbn:nl:ui:32-33158 ; http://library.wur.nl/WebQuery/wurpubs/33158.

MLA Handbook (7th Edition):

Beek, van der, S. “The use of genetic markers in poultry breeding.” 1996. Web. 14 Dec 2019.

Vancouver:

Beek, van der S. The use of genetic markers in poultry breeding. [Internet] [Doctoral dissertation]. Agricultural University; 1996. [cited 2019 Dec 14]. Available from: http://library.wur.nl/WebQuery/wurpubs/33158 ; urn:nbn:nl:ui:32-33158 ; urn:nbn:nl:ui:32-33158 ; http://library.wur.nl/WebQuery/wurpubs/33158.

Council of Science Editors:

Beek, van der S. The use of genetic markers in poultry breeding. [Doctoral Dissertation]. Agricultural University; 1996. Available from: http://library.wur.nl/WebQuery/wurpubs/33158 ; urn:nbn:nl:ui:32-33158 ; urn:nbn:nl:ui:32-33158 ; http://library.wur.nl/WebQuery/wurpubs/33158

6. Eck, van, H.J. Localisation of morphological traits on the genetic map of potato using RFLP and isozyme markers = [Localisatie van morfologische eigenschappen op de genetische kaart van de aardappel door middel van RFLP en isozym merkers].

Degree: 1995, Agricultural University

  The thesis describes the construction of a genetic linkage map of the potato genome, comprising molecular, isozyme and morphological markers. The linkage map is… (more)

Subjects/Keywords: solanum tuberosum; aardappelen; chromosoomkaarten; genkartering; moleculaire genetica; massaselectie; solanum tuberosum; potatoes; chromosome maps; gene mapping; molecular genetics; mass selection

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Eck, van, H. J. (1995). Localisation of morphological traits on the genetic map of potato using RFLP and isozyme markers = [Localisatie van morfologische eigenschappen op de genetische kaart van de aardappel door middel van RFLP en isozym merkers]. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/30440 ; urn:nbn:nl:ui:32-30440 ; urn:nbn:nl:ui:32-30440 ; http://library.wur.nl/WebQuery/wurpubs/30440

Chicago Manual of Style (16th Edition):

Eck, van, H J. “Localisation of morphological traits on the genetic map of potato using RFLP and isozyme markers = [Localisatie van morfologische eigenschappen op de genetische kaart van de aardappel door middel van RFLP en isozym merkers].” 1995. Doctoral Dissertation, Agricultural University. Accessed December 14, 2019. http://library.wur.nl/WebQuery/wurpubs/30440 ; urn:nbn:nl:ui:32-30440 ; urn:nbn:nl:ui:32-30440 ; http://library.wur.nl/WebQuery/wurpubs/30440.

MLA Handbook (7th Edition):

Eck, van, H J. “Localisation of morphological traits on the genetic map of potato using RFLP and isozyme markers = [Localisatie van morfologische eigenschappen op de genetische kaart van de aardappel door middel van RFLP en isozym merkers].” 1995. Web. 14 Dec 2019.

Vancouver:

Eck, van HJ. Localisation of morphological traits on the genetic map of potato using RFLP and isozyme markers = [Localisatie van morfologische eigenschappen op de genetische kaart van de aardappel door middel van RFLP en isozym merkers]. [Internet] [Doctoral dissertation]. Agricultural University; 1995. [cited 2019 Dec 14]. Available from: http://library.wur.nl/WebQuery/wurpubs/30440 ; urn:nbn:nl:ui:32-30440 ; urn:nbn:nl:ui:32-30440 ; http://library.wur.nl/WebQuery/wurpubs/30440.

Council of Science Editors:

Eck, van HJ. Localisation of morphological traits on the genetic map of potato using RFLP and isozyme markers = [Localisatie van morfologische eigenschappen op de genetische kaart van de aardappel door middel van RFLP en isozym merkers]. [Doctoral Dissertation]. Agricultural University; 1995. Available from: http://library.wur.nl/WebQuery/wurpubs/30440 ; urn:nbn:nl:ui:32-30440 ; urn:nbn:nl:ui:32-30440 ; http://library.wur.nl/WebQuery/wurpubs/30440

7. Jacobs, J.M.E. A genetic map of potato : construction and applications.

Degree: 1995, Agricultural University

  This thesis describes the construction of an integrated genetic map of potato (Solanum tuberosum L.) using molecular, morphological and isozyme markers. A general method… (more)

Subjects/Keywords: solanum tuberosum; aardappelen; chromosoomkaarten; genkartering; moleculaire genetica; plantenveredeling; ziekteresistentie; plaagresistentie; solanum tuberosum; potatoes; chromosome maps; gene mapping; molecular genetics; plant breeding; disease resistance; pest resistance

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APA (6th Edition):

Jacobs, J. M. E. (1995). A genetic map of potato : construction and applications. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/29849 ; urn:nbn:nl:ui:32-29849 ; urn:nbn:nl:ui:32-29849 ; http://library.wur.nl/WebQuery/wurpubs/29849

Chicago Manual of Style (16th Edition):

Jacobs, J M E. “A genetic map of potato : construction and applications.” 1995. Doctoral Dissertation, Agricultural University. Accessed December 14, 2019. http://library.wur.nl/WebQuery/wurpubs/29849 ; urn:nbn:nl:ui:32-29849 ; urn:nbn:nl:ui:32-29849 ; http://library.wur.nl/WebQuery/wurpubs/29849.

MLA Handbook (7th Edition):

Jacobs, J M E. “A genetic map of potato : construction and applications.” 1995. Web. 14 Dec 2019.

Vancouver:

Jacobs JME. A genetic map of potato : construction and applications. [Internet] [Doctoral dissertation]. Agricultural University; 1995. [cited 2019 Dec 14]. Available from: http://library.wur.nl/WebQuery/wurpubs/29849 ; urn:nbn:nl:ui:32-29849 ; urn:nbn:nl:ui:32-29849 ; http://library.wur.nl/WebQuery/wurpubs/29849.

Council of Science Editors:

Jacobs JME. A genetic map of potato : construction and applications. [Doctoral Dissertation]. Agricultural University; 1995. Available from: http://library.wur.nl/WebQuery/wurpubs/29849 ; urn:nbn:nl:ui:32-29849 ; urn:nbn:nl:ui:32-29849 ; http://library.wur.nl/WebQuery/wurpubs/29849

8. Jansen, R.C. Genetic mapping of quantitative trait loci in plants : a novel statistical approach.

Degree: 1995, Agricultural University

  Quantitative variation is a feature of many important traits such as yield, quality and disease resistance in crop plants and farm animals, and diseases… (more)

Subjects/Keywords: chromosoomkaarten; genkartering; genen; moleculaire genetica; Kwantitatieve- en populatiegenetica; chromosome maps; gene mapping; genes; molecular genetics; Population and Quantitative Genetics; cum laude

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APA (6th Edition):

Jansen, R. C. (1995). Genetic mapping of quantitative trait loci in plants : a novel statistical approach. (Doctoral Dissertation). Agricultural University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/28703 ; urn:nbn:nl:ui:32-28703 ; urn:nbn:nl:ui:32-28703 ; http://library.wur.nl/WebQuery/wurpubs/28703

Chicago Manual of Style (16th Edition):

Jansen, R C. “Genetic mapping of quantitative trait loci in plants : a novel statistical approach.” 1995. Doctoral Dissertation, Agricultural University. Accessed December 14, 2019. http://library.wur.nl/WebQuery/wurpubs/28703 ; urn:nbn:nl:ui:32-28703 ; urn:nbn:nl:ui:32-28703 ; http://library.wur.nl/WebQuery/wurpubs/28703.

MLA Handbook (7th Edition):

Jansen, R C. “Genetic mapping of quantitative trait loci in plants : a novel statistical approach.” 1995. Web. 14 Dec 2019.

Vancouver:

Jansen RC. Genetic mapping of quantitative trait loci in plants : a novel statistical approach. [Internet] [Doctoral dissertation]. Agricultural University; 1995. [cited 2019 Dec 14]. Available from: http://library.wur.nl/WebQuery/wurpubs/28703 ; urn:nbn:nl:ui:32-28703 ; urn:nbn:nl:ui:32-28703 ; http://library.wur.nl/WebQuery/wurpubs/28703.

Council of Science Editors:

Jansen RC. Genetic mapping of quantitative trait loci in plants : a novel statistical approach. [Doctoral Dissertation]. Agricultural University; 1995. Available from: http://library.wur.nl/WebQuery/wurpubs/28703 ; urn:nbn:nl:ui:32-28703 ; urn:nbn:nl:ui:32-28703 ; http://library.wur.nl/WebQuery/wurpubs/28703

9. Madhu, K. Genotoxicity Studies on Liza Parsia and Mugil Cephalus.

Degree: 1995, Cochin University of Science and Technology

Subjects/Keywords: Genotoxicity; Liza Parsia; Mugil Cephalus; Chromosome; Mullets

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APA (6th Edition):

Madhu, K. (1995). Genotoxicity Studies on Liza Parsia and Mugil Cephalus. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/1895

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Madhu, K. “Genotoxicity Studies on Liza Parsia and Mugil Cephalus.” 1995. Thesis, Cochin University of Science and Technology. Accessed December 14, 2019. http://dyuthi.cusat.ac.in/purl/1895.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Madhu, K. “Genotoxicity Studies on Liza Parsia and Mugil Cephalus.” 1995. Web. 14 Dec 2019.

Vancouver:

Madhu K. Genotoxicity Studies on Liza Parsia and Mugil Cephalus. [Internet] [Thesis]. Cochin University of Science and Technology; 1995. [cited 2019 Dec 14]. Available from: http://dyuthi.cusat.ac.in/purl/1895.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Madhu K. Genotoxicity Studies on Liza Parsia and Mugil Cephalus. [Thesis]. Cochin University of Science and Technology; 1995. Available from: http://dyuthi.cusat.ac.in/purl/1895

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

10. Vosse, Esther van de. Positional Cloning in Xp22: towards the isolation of the gene involved in X-linked retinoschisis.

Degree: 1998, Department of Human Genetics, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 The study was aimed at the positional cloning of disease genes in Xp22.1-p22.2. To this end a YAC contig covering this region was constructed. To… (more)

Subjects/Keywords: X chromosome; genetics; positional cloning; X-linked retinoschisis; Xp22; exon trapping; keratosis follicularis spinulosa decalvans; X-linked retinitis pigmentosa; X chromosome; genetics; positional cloning; X-linked retinoschisis; Xp22; exon trapping; keratosis follicularis spinulosa decalvans; X-linked retinitis pigmentosa

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APA (6th Edition):

Vosse, E. v. d. (1998). Positional Cloning in Xp22: towards the isolation of the gene involved in X-linked retinoschisis. (Doctoral Dissertation). Department of Human Genetics, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/28328

Chicago Manual of Style (16th Edition):

Vosse, Esther van de. “Positional Cloning in Xp22: towards the isolation of the gene involved in X-linked retinoschisis.” 1998. Doctoral Dissertation, Department of Human Genetics, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed December 14, 2019. http://hdl.handle.net/1887/28328.

MLA Handbook (7th Edition):

Vosse, Esther van de. “Positional Cloning in Xp22: towards the isolation of the gene involved in X-linked retinoschisis.” 1998. Web. 14 Dec 2019.

Vancouver:

Vosse Evd. Positional Cloning in Xp22: towards the isolation of the gene involved in X-linked retinoschisis. [Internet] [Doctoral dissertation]. Department of Human Genetics, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 1998. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/1887/28328.

Council of Science Editors:

Vosse Evd. Positional Cloning in Xp22: towards the isolation of the gene involved in X-linked retinoschisis. [Doctoral Dissertation]. Department of Human Genetics, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 1998. Available from: http://hdl.handle.net/1887/28328


ETH Zürich

11. Kovács, Beáta Zsuzsanna. Der synaptonemale Komplex bei weiblicher Kaninchen und Rinderföten im Vergleich zu zytogenetischen Erscheinungen.

Degree: 1999, ETH Zürich

Subjects/Keywords: GESCHLECHTSCHROMOSOMEN (CYTOLOGIE); MEIOSE (CYTOLOGIE); SYNAPSIS + CHROMOSOMENPAARUNG + ZYGONEMA (MEIOTISCHE ZELLTEILUNG); BOS (ZOOLOGIE); ORYCTOLAGUS (ZOOLOGIE); SEX CHROMOSOMES (CYTOLOGY); MEIOSIS (CYTOLOGY); SYNAPSIS + CHROMOSOME PAIRING + ZYGONEMA (MEIOTIC CELL DIVISION); BOS (ZOOLOGY); ORYCTOLAGUS (ZOOLOGY); info:eu-repo/classification/ddc/570; Life sciences

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kovács, B. Z. (1999). Der synaptonemale Komplex bei weiblicher Kaninchen und Rinderföten im Vergleich zu zytogenetischen Erscheinungen. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/144440

Chicago Manual of Style (16th Edition):

Kovács, Beáta Zsuzsanna. “Der synaptonemale Komplex bei weiblicher Kaninchen und Rinderföten im Vergleich zu zytogenetischen Erscheinungen.” 1999. Doctoral Dissertation, ETH Zürich. Accessed December 14, 2019. http://hdl.handle.net/20.500.11850/144440.

MLA Handbook (7th Edition):

Kovács, Beáta Zsuzsanna. “Der synaptonemale Komplex bei weiblicher Kaninchen und Rinderföten im Vergleich zu zytogenetischen Erscheinungen.” 1999. Web. 14 Dec 2019.

Vancouver:

Kovács BZ. Der synaptonemale Komplex bei weiblicher Kaninchen und Rinderföten im Vergleich zu zytogenetischen Erscheinungen. [Internet] [Doctoral dissertation]. ETH Zürich; 1999. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/20.500.11850/144440.

Council of Science Editors:

Kovács BZ. Der synaptonemale Komplex bei weiblicher Kaninchen und Rinderföten im Vergleich zu zytogenetischen Erscheinungen. [Doctoral Dissertation]. ETH Zürich; 1999. Available from: http://hdl.handle.net/20.500.11850/144440


Indian Institute of Science

12. Saifi, G Mustafa. Studies On Human Sex Chromosomes And Sex Determination.

Degree: 1999, Indian Institute of Science

Subjects/Keywords: Genetic Sex Determination; Human Sex Chromosomes; Human Gene; Human Sex Determination; Human X Chromosome; SRY Gene; Planococcus lilacinus; sY116; Human Physiology

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APA (6th Edition):

Saifi, G. M. (1999). Studies On Human Sex Chromosomes And Sex Determination. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2388

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Saifi, G Mustafa. “Studies On Human Sex Chromosomes And Sex Determination.” 1999. Thesis, Indian Institute of Science. Accessed December 14, 2019. http://hdl.handle.net/2005/2388.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Saifi, G Mustafa. “Studies On Human Sex Chromosomes And Sex Determination.” 1999. Web. 14 Dec 2019.

Vancouver:

Saifi GM. Studies On Human Sex Chromosomes And Sex Determination. [Internet] [Thesis]. Indian Institute of Science; 1999. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/2005/2388.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Saifi GM. Studies On Human Sex Chromosomes And Sex Determination. [Thesis]. Indian Institute of Science; 1999. Available from: http://hdl.handle.net/2005/2388

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

13. Saifi, G Mustafa. Studies On Human Sex Chromosomes And Sex Determination.

Degree: 1999, Indian Institute of Science

Subjects/Keywords: Genetic Sex Determination; Human Sex Chromosomes; Human Gene; Human Sex Determination; Human X Chromosome; SRY Gene; Planococcus lilacinus; sY116; Human Physiology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Saifi, G. M. (1999). Studies On Human Sex Chromosomes And Sex Determination. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/2388 ; http://etd.ncsi.iisc.ernet.in/abstracts/3071/G15589-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Saifi, G Mustafa. “Studies On Human Sex Chromosomes And Sex Determination.” 1999. Thesis, Indian Institute of Science. Accessed December 14, 2019. http://etd.iisc.ernet.in/handle/2005/2388 ; http://etd.ncsi.iisc.ernet.in/abstracts/3071/G15589-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Saifi, G Mustafa. “Studies On Human Sex Chromosomes And Sex Determination.” 1999. Web. 14 Dec 2019.

Vancouver:

Saifi GM. Studies On Human Sex Chromosomes And Sex Determination. [Internet] [Thesis]. Indian Institute of Science; 1999. [cited 2019 Dec 14]. Available from: http://etd.iisc.ernet.in/handle/2005/2388 ; http://etd.ncsi.iisc.ernet.in/abstracts/3071/G15589-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Saifi GM. Studies On Human Sex Chromosomes And Sex Determination. [Thesis]. Indian Institute of Science; 1999. Available from: http://etd.iisc.ernet.in/handle/2005/2388 ; http://etd.ncsi.iisc.ernet.in/abstracts/3071/G15589-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Massey University

14. Harding, Katherine Mary. Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25.

Degree: MS, Genetics, 1996, Massey University

 The chromosomes of human peripheral blood lymphocytes were analysed for sister chromatid exchanges (SCEs) and structural aberrations and correlated to cigarette smoking habits of 15… (more)

Subjects/Keywords: Human chromosome abnormalities; Smoking  – Health aspects; Women  – Tobacco use; Vanillin  – Health aspects

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APA (6th Edition):

Harding, K. M. (1996). Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/10280

Chicago Manual of Style (16th Edition):

Harding, Katherine Mary. “Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25.” 1996. Masters Thesis, Massey University. Accessed December 14, 2019. http://hdl.handle.net/10179/10280.

MLA Handbook (7th Edition):

Harding, Katherine Mary. “Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25.” 1996. Web. 14 Dec 2019.

Vancouver:

Harding KM. Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25. [Internet] [Masters thesis]. Massey University; 1996. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/10179/10280.

Council of Science Editors:

Harding KM. Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25. [Masters Thesis]. Massey University; 1996. Available from: http://hdl.handle.net/10179/10280


McGill University

15. Fernandes, Maria J. G. Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus.

Degree: PhD, Department of Biology, 1995, McGill University

Note:

Tay-Sachs disease (TSD) is a recessively inherited disorder characterized by the pathological accumulation of GM 2 ganglioside in neuronal cells. Mutations in the HEXA… (more)

Subjects/Keywords: Tay-Sachs disease.; Human chromosome abnormalities  – Diagnosis.

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APA (6th Edition):

Fernandes, M. J. G. (1995). Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile156990.pdf

Chicago Manual of Style (16th Edition):

Fernandes, Maria J G. “Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus.” 1995. Doctoral Dissertation, McGill University. Accessed December 14, 2019. http://digitool.library.mcgill.ca/thesisfile156990.pdf.

MLA Handbook (7th Edition):

Fernandes, Maria J G. “Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus.” 1995. Web. 14 Dec 2019.

Vancouver:

Fernandes MJG. Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus. [Internet] [Doctoral dissertation]. McGill University; 1995. [cited 2019 Dec 14]. Available from: http://digitool.library.mcgill.ca/thesisfile156990.pdf.

Council of Science Editors:

Fernandes MJG. Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus. [Doctoral Dissertation]. McGill University; 1995. Available from: http://digitool.library.mcgill.ca/thesisfile156990.pdf


McGill University

16. Vasiliou, Denise Marie. Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome.

Degree: MS, Department of Biology., 1996, McGill University

 The human androgen receptor (hAR) is a ligand-activated, nuclear transcription factor. Mutations affecting the formation and/or action of the hAR cause androgen insensitivity syndrome (AIS).… (more)

Subjects/Keywords: Androgens  – Receptors.; Exons (Genetics); Sex differentiation disorders.; X chromosome  – Abnormalities.

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APA (6th Edition):

Vasiliou, D. M. (1996). Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile27431.pdf

Chicago Manual of Style (16th Edition):

Vasiliou, Denise Marie. “Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome.” 1996. Masters Thesis, McGill University. Accessed December 14, 2019. http://digitool.library.mcgill.ca/thesisfile27431.pdf.

MLA Handbook (7th Edition):

Vasiliou, Denise Marie. “Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome.” 1996. Web. 14 Dec 2019.

Vancouver:

Vasiliou DM. Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome. [Internet] [Masters thesis]. McGill University; 1996. [cited 2019 Dec 14]. Available from: http://digitool.library.mcgill.ca/thesisfile27431.pdf.

Council of Science Editors:

Vasiliou DM. Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome. [Masters Thesis]. McGill University; 1996. Available from: http://digitool.library.mcgill.ca/thesisfile27431.pdf


McGill University

17. Kazemi-Esfarjani, Parsa. Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations.

Degree: PhD, Department of Biology., 1996, McGill University

The human androgen receptor (hAR) is a ligand-activated transcription factor, and like other nuclear receptors, consists of a N-terminal modulatory domain, a central DNA-binding domain,… (more)

Subjects/Keywords: Androgens  – Receptors.; Sex differentiation disorders.; X chromosome  – Abnormalities.

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APA (6th Edition):

Kazemi-Esfarjani, P. (1996). Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile42065.pdf

Chicago Manual of Style (16th Edition):

Kazemi-Esfarjani, Parsa. “Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations.” 1996. Doctoral Dissertation, McGill University. Accessed December 14, 2019. http://digitool.library.mcgill.ca/thesisfile42065.pdf.

MLA Handbook (7th Edition):

Kazemi-Esfarjani, Parsa. “Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations.” 1996. Web. 14 Dec 2019.

Vancouver:

Kazemi-Esfarjani P. Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations. [Internet] [Doctoral dissertation]. McGill University; 1996. [cited 2019 Dec 14]. Available from: http://digitool.library.mcgill.ca/thesisfile42065.pdf.

Council of Science Editors:

Kazemi-Esfarjani P. Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations. [Doctoral Dissertation]. McGill University; 1996. Available from: http://digitool.library.mcgill.ca/thesisfile42065.pdf


McGill University

18. Shkolny, Dana. Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome.

Degree: MS, Department of Biology., 1995, McGill University

 This work proves the pathogenicity of four substitution mutations in the androgen-binding domain of the human androgen receptor (hAR) gene of four subjects with varying… (more)

Subjects/Keywords: Androgens  – Receptors; Sex differentiation disorders; X chromosome  – Abnormalities

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APA (6th Edition):

Shkolny, D. (1995). Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile23299.pdf

Chicago Manual of Style (16th Edition):

Shkolny, Dana. “Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome.” 1995. Masters Thesis, McGill University. Accessed December 14, 2019. http://digitool.library.mcgill.ca/thesisfile23299.pdf.

MLA Handbook (7th Edition):

Shkolny, Dana. “Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome.” 1995. Web. 14 Dec 2019.

Vancouver:

Shkolny D. Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome. [Internet] [Masters thesis]. McGill University; 1995. [cited 2019 Dec 14]. Available from: http://digitool.library.mcgill.ca/thesisfile23299.pdf.

Council of Science Editors:

Shkolny D. Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome. [Masters Thesis]. McGill University; 1995. Available from: http://digitool.library.mcgill.ca/thesisfile23299.pdf


McGill University

19. Demczuk, Suzanne. Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions.

Degree: PhD, Department of Biology., 1995, McGill University

DiGeorge syndrome (DGS) is a developmental defect associated with deletions in chromosomal region 22q11.2. Recently, other syndromes (Velo-Cardio-Facial syndrome, Conotruncal Anomaly Face syndrome, isolated conotruncal… (more)

Subjects/Keywords: Human chromosome abnormalities; Human cytogenetics

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Demczuk, S. (1995). Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile28726.pdf

Chicago Manual of Style (16th Edition):

Demczuk, Suzanne. “Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions.” 1995. Doctoral Dissertation, McGill University. Accessed December 14, 2019. http://digitool.library.mcgill.ca/thesisfile28726.pdf.

MLA Handbook (7th Edition):

Demczuk, Suzanne. “Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions.” 1995. Web. 14 Dec 2019.

Vancouver:

Demczuk S. Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions. [Internet] [Doctoral dissertation]. McGill University; 1995. [cited 2019 Dec 14]. Available from: http://digitool.library.mcgill.ca/thesisfile28726.pdf.

Council of Science Editors:

Demczuk S. Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions. [Doctoral Dissertation]. McGill University; 1995. Available from: http://digitool.library.mcgill.ca/thesisfile28726.pdf


Michigan State University

20. Zubair, Qaisra. An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16.

Degree: MS, Medical Technology Program and Department of Pediatrics and Human Development, 1996, Michigan State University

Subjects/Keywords: Human chromosome abnormalities; Chromosomes – Analysis; Premature infants; Fetal growth retardation – Genetic aspects

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APA (6th Edition):

Zubair, Q. (1996). An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:26756

Chicago Manual of Style (16th Edition):

Zubair, Qaisra. “An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16.” 1996. Masters Thesis, Michigan State University. Accessed December 14, 2019. http://etd.lib.msu.edu/islandora/object/etd:26756.

MLA Handbook (7th Edition):

Zubair, Qaisra. “An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16.” 1996. Web. 14 Dec 2019.

Vancouver:

Zubair Q. An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16. [Internet] [Masters thesis]. Michigan State University; 1996. [cited 2019 Dec 14]. Available from: http://etd.lib.msu.edu/islandora/object/etd:26756.

Council of Science Editors:

Zubair Q. An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16. [Masters Thesis]. Michigan State University; 1996. Available from: http://etd.lib.msu.edu/islandora/object/etd:26756


Michigan State University

21. Liang, Yong. Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness].

Degree: PhD, Graduate Program in Genetics, 1999, Michigan State University

Subjects/Keywords: Deafness – Genetic aspects; Gene mapping; Human chromosome abnormalities

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APA (6th Edition):

Liang, Y. (1999). Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:27758

Chicago Manual of Style (16th Edition):

Liang, Yong. “Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness].” 1999. Doctoral Dissertation, Michigan State University. Accessed December 14, 2019. http://etd.lib.msu.edu/islandora/object/etd:27758.

MLA Handbook (7th Edition):

Liang, Yong. “Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness].” 1999. Web. 14 Dec 2019.

Vancouver:

Liang Y. Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]. [Internet] [Doctoral dissertation]. Michigan State University; 1999. [cited 2019 Dec 14]. Available from: http://etd.lib.msu.edu/islandora/object/etd:27758.

Council of Science Editors:

Liang Y. Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]. [Doctoral Dissertation]. Michigan State University; 1999. Available from: http://etd.lib.msu.edu/islandora/object/etd:27758

22. Van Dyk, Qinuo Fan. Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men.

Degree: PhD, 1997, Old Dominion University

  The human hemizona has been demonstrated to select spermatozoa with good motility, normal morphology, and the capacity to undergo the zona-induced acrosomal reaction. The… (more)

Subjects/Keywords: Sex chromosome ratios; Aneuploidy rates; Zona pellucida; Spermatozoa; Genetics; Molecular Biology

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APA (6th Edition):

Van Dyk, Q. F. (1997). Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men. (Doctoral Dissertation). Old Dominion University. Retrieved from 9780591631845 ; https://digitalcommons.odu.edu/biomedicalsciences_etds/86

Chicago Manual of Style (16th Edition):

Van Dyk, Qinuo Fan. “Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men.” 1997. Doctoral Dissertation, Old Dominion University. Accessed December 14, 2019. 9780591631845 ; https://digitalcommons.odu.edu/biomedicalsciences_etds/86.

MLA Handbook (7th Edition):

Van Dyk, Qinuo Fan. “Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men.” 1997. Web. 14 Dec 2019.

Vancouver:

Van Dyk QF. Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men. [Internet] [Doctoral dissertation]. Old Dominion University; 1997. [cited 2019 Dec 14]. Available from: 9780591631845 ; https://digitalcommons.odu.edu/biomedicalsciences_etds/86.

Council of Science Editors:

Van Dyk QF. Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men. [Doctoral Dissertation]. Old Dominion University; 1997. Available from: 9780591631845 ; https://digitalcommons.odu.edu/biomedicalsciences_etds/86

23. Toth-Fejel, SuEllen June. Cytogenetic and molecular studies of chromosome 15 abnormalities and imprinting in Prader-Willi and Angelman syndromes.

Degree: PhD, 1996, Oregon Health Sciences University

Subjects/Keywords: Chromosome Aberrations; Chromosomes, Human, Pair 15; Prader-Willi Syndrome  – genetics; Angelman Syndrome  – genetics; Genomic Imprinting

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APA (6th Edition):

Toth-Fejel, S. J. (1996). Cytogenetic and molecular studies of chromosome 15 abnormalities and imprinting in Prader-Willi and Angelman syndromes. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4FF3QKS ; http://digitalcommons.ohsu.edu/etd/2690

Chicago Manual of Style (16th Edition):

Toth-Fejel, SuEllen June. “Cytogenetic and molecular studies of chromosome 15 abnormalities and imprinting in Prader-Willi and Angelman syndromes.” 1996. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 14, 2019. doi:10.6083/M4FF3QKS ; http://digitalcommons.ohsu.edu/etd/2690.

MLA Handbook (7th Edition):

Toth-Fejel, SuEllen June. “Cytogenetic and molecular studies of chromosome 15 abnormalities and imprinting in Prader-Willi and Angelman syndromes.” 1996. Web. 14 Dec 2019.

Vancouver:

Toth-Fejel SJ. Cytogenetic and molecular studies of chromosome 15 abnormalities and imprinting in Prader-Willi and Angelman syndromes. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1996. [cited 2019 Dec 14]. Available from: doi:10.6083/M4FF3QKS ; http://digitalcommons.ohsu.edu/etd/2690.

Council of Science Editors:

Toth-Fejel SJ. Cytogenetic and molecular studies of chromosome 15 abnormalities and imprinting in Prader-Willi and Angelman syndromes. [Doctoral Dissertation]. Oregon Health Sciences University; 1996. Available from: doi:10.6083/M4FF3QKS ; http://digitalcommons.ohsu.edu/etd/2690

24. Gault, Judith M. Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias.

Degree: PhD, 1995, Oregon Health Sciences University

Subjects/Keywords: Ectodermal Dysplasia  – genetics; X Chromosome; Cloning, Molecular; Chromosome Mapping

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APA (6th Edition):

Gault, J. M. (1995). Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4F47MC8 ; http://digitalcommons.ohsu.edu/etd/2752

Chicago Manual of Style (16th Edition):

Gault, Judith M. “Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias.” 1995. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 14, 2019. doi:10.6083/M4F47MC8 ; http://digitalcommons.ohsu.edu/etd/2752.

MLA Handbook (7th Edition):

Gault, Judith M. “Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias.” 1995. Web. 14 Dec 2019.

Vancouver:

Gault JM. Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1995. [cited 2019 Dec 14]. Available from: doi:10.6083/M4F47MC8 ; http://digitalcommons.ohsu.edu/etd/2752.

Council of Science Editors:

Gault JM. Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias. [Doctoral Dissertation]. Oregon Health Sciences University; 1995. Available from: doi:10.6083/M4F47MC8 ; http://digitalcommons.ohsu.edu/etd/2752

25. Metten, Pamela. Genetics of acute ethanol and benzodiazepine withdrawal severity.

Degree: PhD, 1996, Oregon Health Sciences University

Subjects/Keywords: Substance Withdrawal Syndrome  – genetics; Ethanol; Benzodiazepines; Chromosome Mapping; Mice, Inbred Strains

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APA (6th Edition):

Metten, P. (1996). Genetics of acute ethanol and benzodiazepine withdrawal severity. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4348HMF ; http://digitalcommons.ohsu.edu/etd/2685

Chicago Manual of Style (16th Edition):

Metten, Pamela. “Genetics of acute ethanol and benzodiazepine withdrawal severity.” 1996. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 14, 2019. doi:10.6083/M4348HMF ; http://digitalcommons.ohsu.edu/etd/2685.

MLA Handbook (7th Edition):

Metten, Pamela. “Genetics of acute ethanol and benzodiazepine withdrawal severity.” 1996. Web. 14 Dec 2019.

Vancouver:

Metten P. Genetics of acute ethanol and benzodiazepine withdrawal severity. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1996. [cited 2019 Dec 14]. Available from: doi:10.6083/M4348HMF ; http://digitalcommons.ohsu.edu/etd/2685.

Council of Science Editors:

Metten P. Genetics of acute ethanol and benzodiazepine withdrawal severity. [Doctoral Dissertation]. Oregon Health Sciences University; 1996. Available from: doi:10.6083/M4348HMF ; http://digitalcommons.ohsu.edu/etd/2685

26. Hain, Heather S. Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay.

Degree: PhD, 1999, Oregon Health Sciences University

Subjects/Keywords: Nociceptors  – drug effects; Chromosome Mapping; Morphine; Narcotic Antagonists; Analgesia; Mice, Inbred Strains

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APA (6th Edition):

Hain, H. S. (1999). Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4HX1B09 ; http://digitalcommons.ohsu.edu/etd/3356

Chicago Manual of Style (16th Edition):

Hain, Heather S. “Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay.” 1999. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 14, 2019. doi:10.6083/M4HX1B09 ; http://digitalcommons.ohsu.edu/etd/3356.

MLA Handbook (7th Edition):

Hain, Heather S. “Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay.” 1999. Web. 14 Dec 2019.

Vancouver:

Hain HS. Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1999. [cited 2019 Dec 14]. Available from: doi:10.6083/M4HX1B09 ; http://digitalcommons.ohsu.edu/etd/3356.

Council of Science Editors:

Hain HS. Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay. [Doctoral Dissertation]. Oregon Health Sciences University; 1999. Available from: doi:10.6083/M4HX1B09 ; http://digitalcommons.ohsu.edu/etd/3356

27. Angeli-Gade, Sandra Joe. Genetic and behavioral analysis of methamphetamine-induced anorexia in mice.

Degree: PhD, 1996, Oregon Health Sciences University

Subjects/Keywords: Methamphetamine  – toxicity; Anorexia  – chemically induced; Anorexia  – genetics; Behavior, Animal  – drug effects; Chromosome Mapping; Mice, Inbred Strains

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APA (6th Edition):

Angeli-Gade, S. J. (1996). Genetic and behavioral analysis of methamphetamine-induced anorexia in mice. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4SQ8XNX ; http://digitalcommons.ohsu.edu/etd/2695

Chicago Manual of Style (16th Edition):

Angeli-Gade, Sandra Joe. “Genetic and behavioral analysis of methamphetamine-induced anorexia in mice.” 1996. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 14, 2019. doi:10.6083/M4SQ8XNX ; http://digitalcommons.ohsu.edu/etd/2695.

MLA Handbook (7th Edition):

Angeli-Gade, Sandra Joe. “Genetic and behavioral analysis of methamphetamine-induced anorexia in mice.” 1996. Web. 14 Dec 2019.

Vancouver:

Angeli-Gade SJ. Genetic and behavioral analysis of methamphetamine-induced anorexia in mice. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1996. [cited 2019 Dec 14]. Available from: doi:10.6083/M4SQ8XNX ; http://digitalcommons.ohsu.edu/etd/2695.

Council of Science Editors:

Angeli-Gade SJ. Genetic and behavioral analysis of methamphetamine-induced anorexia in mice. [Doctoral Dissertation]. Oregon Health Sciences University; 1996. Available from: doi:10.6083/M4SQ8XNX ; http://digitalcommons.ohsu.edu/etd/2695

28. Rupp, Paul A. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.

Degree: PhD, 1999, Oregon Health Sciences University

Subjects/Keywords: Base Sequence; Blotting, Western; Heart Defects, Congenital; Chromosome Deletion; Membrane Proteins  – genetics

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APA (6th Edition):

Rupp, P. A. (1999). Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341

Chicago Manual of Style (16th Edition):

Rupp, Paul A. “Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.” 1999. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 14, 2019. doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341.

MLA Handbook (7th Edition):

Rupp, Paul A. “Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.” 1999. Web. 14 Dec 2019.

Vancouver:

Rupp PA. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1999. [cited 2019 Dec 14]. Available from: doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341.

Council of Science Editors:

Rupp PA. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. [Doctoral Dissertation]. Oregon Health Sciences University; 1999. Available from: doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341


Oregon State University

29. Gale, William L. Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone.

Degree: MS, Fisheries Science, 1996, Oregon State University

Subjects/Keywords: Chromosome inversions

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APA (6th Edition):

Gale, W. L. (1996). Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/34815

Chicago Manual of Style (16th Edition):

Gale, William L. “Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone.” 1996. Masters Thesis, Oregon State University. Accessed December 14, 2019. http://hdl.handle.net/1957/34815.

MLA Handbook (7th Edition):

Gale, William L. “Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone.” 1996. Web. 14 Dec 2019.

Vancouver:

Gale WL. Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone. [Internet] [Masters thesis]. Oregon State University; 1996. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/1957/34815.

Council of Science Editors:

Gale WL. Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone. [Masters Thesis]. Oregon State University; 1996. Available from: http://hdl.handle.net/1957/34815


University of Adelaide

30. Donnelly, Andrew James. The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly.

Degree: 1997, University of Adelaide

 The aim of the project presented in this thesis is to isolate microsatellite markers and to construct a high resolution genetic map of the human… (more)

Subjects/Keywords: Human gene mapping.; Genetics Research.; Fragile X syndrome.; X chromosome Abnormalities.; Mental retardation.

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APA (6th Edition):

Donnelly, A. J. (1997). The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19022

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Donnelly, Andrew James. “The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly.” 1997. Thesis, University of Adelaide. Accessed December 14, 2019. http://hdl.handle.net/2440/19022.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Donnelly, Andrew James. “The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly.” 1997. Web. 14 Dec 2019.

Vancouver:

Donnelly AJ. The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly. [Internet] [Thesis]. University of Adelaide; 1997. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/2440/19022.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Donnelly AJ. The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly. [Thesis]. University of Adelaide; 1997. Available from: http://hdl.handle.net/2440/19022

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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