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H Ostrer

Showing results (61-70 of 83) with videos related to

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Nature|December 23, 1982
Abnormal RNA processing due to the exon mutation of beta E-globin geneS H Orkin, H H Kazazian, S E Antonarakis, et al.
American Journal of Medical Genetics|March 1, 1990
Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprintingC A Williams, R T Zori, J W Stone, et al.
Gynecologic Oncology|June 16, 2004
Genetic variants in SOD2, MPO, and NQO1, and risk of ovarian cancerS H Olson, M D A Carlson, H Ostrer, et al.
American Journal of Human Genetics|March 1, 1993
Insurance and genetic testing: where are we now?H Ostrer, W Allen, L A Crandall, et al.
American Journal of Human Genetics|January 1, 1990
Regional evaluation of DNA diagnostic laboratoriesK J Matteson, P E Barker, G C Kaplan, et al.
Human Genetics|January 1, 1985
A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locusK J Matteson, H Ostrer, A Chakravarti, et al.
Archives of Family Medicine|November 1, 1993
Ethical and practical implications of the human genome initiative for family medicineS V McCrary, B Allen, R Moseley, et al.
Clinical Genetics|June 6, 2003
Mapping a gene for 46,XY gonadal dysgenesis by linkage analysisD Jawaheer, S-H H Juo, C Le Caignec, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Linkage analysis of a kindred with inherited 46,XY partial gonadal dysgenesisJ S Fuqua, E S Sher, P Y Fechner, et al.
Human Genetics|May 1, 1997
Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotypeR Veitia, A Ion, S Barbaux, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Nature|December 23, 1982
Abnormal RNA processing due to the exon mutation of beta E-globin geneS H Orkin, H H Kazazian, S E Antonarakis, et al.
American Journal of Medical Genetics|March 1, 1990
Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprintingC A Williams, R T Zori, J W Stone, et al.
Gynecologic Oncology|June 16, 2004
Genetic variants in SOD2, MPO, and NQO1, and risk of ovarian cancerS H Olson, M D A Carlson, H Ostrer, et al.
American Journal of Human Genetics|March 1, 1993
Insurance and genetic testing: where are we now?H Ostrer, W Allen, L A Crandall, et al.
American Journal of Human Genetics|January 1, 1990
Regional evaluation of DNA diagnostic laboratoriesK J Matteson, P E Barker, G C Kaplan, et al.
Human Genetics|January 1, 1985
A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locusK J Matteson, H Ostrer, A Chakravarti, et al.
Archives of Family Medicine|November 1, 1993
Ethical and practical implications of the human genome initiative for family medicineS V McCrary, B Allen, R Moseley, et al.
Clinical Genetics|June 6, 2003
Mapping a gene for 46,XY gonadal dysgenesis by linkage analysisD Jawaheer, S-H H Juo, C Le Caignec, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Linkage analysis of a kindred with inherited 46,XY partial gonadal dysgenesisJ S Fuqua, E S Sher, P Y Fechner, et al.
Human Genetics|May 1, 1997
Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotypeR Veitia, A Ion, S Barbaux, et al.
Pageof 9