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A R Zinn

Showing results (21-30 of 32) with videos related to

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Clinical Genetics|January 24, 1998
Del (X)(p21.2) in a mother and two daughters with variable ovarian functionA R Zinn, B Ouyang, J L Ross, et al.
Molecular and Cellular Biology|April 1, 1994
Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomesA R Zinn, R K Alagappan, L G Brown, et al.
American Journal of Medical Genetics|May 2, 1997
Prune-belly syndrome and other anomalies in a stillborn fetus with a ring X chromosome lacking XISTD R Guillén, A Lowichik, N R Schneider, et al.
American Journal of Medical Genetics|August 15, 2001
A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from his mother and neurofibromatosis type 1 from his fatherF Wei, S Cheng, N Badie, et al.
Human Molecular Genetics|June 17, 1999
New gene family defined by MORC, a nuclear protein required for mouse spermatogenesisN Inoue, K D Hess, R W Moreadith, et al.
Genomics|December 1, 1991
Inactivation of the Rps4 gene on the mouse X chromosomeA R Zinn, S L Bressler, P Beer-Romero, et al.
The British Journal of Dermatology|April 14, 2017
Evolution of the skin manifestations of X-linked pigmentary reticulate disorderP Starokadomskyy, L Sifuentes-Dominguez, T Gemelli, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 1998
Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouseM L Watson, A R Zinn, N Inoue, et al.
American Journal of Human Genetics|December 5, 1998
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1A R Zinn, V S Tonk, Z Chen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
Phenotypes Associated with SHOX DeficiencyJ L Ross, C Scott, P Marttila, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Clinical Genetics|January 24, 1998
Del (X)(p21.2) in a mother and two daughters with variable ovarian functionA R Zinn, B Ouyang, J L Ross, et al.
Molecular and Cellular Biology|April 1, 1994
Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomesA R Zinn, R K Alagappan, L G Brown, et al.
American Journal of Medical Genetics|May 2, 1997
Prune-belly syndrome and other anomalies in a stillborn fetus with a ring X chromosome lacking XISTD R Guillén, A Lowichik, N R Schneider, et al.
American Journal of Medical Genetics|August 15, 2001
A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from his mother and neurofibromatosis type 1 from his fatherF Wei, S Cheng, N Badie, et al.
Human Molecular Genetics|June 17, 1999
New gene family defined by MORC, a nuclear protein required for mouse spermatogenesisN Inoue, K D Hess, R W Moreadith, et al.
Genomics|December 1, 1991
Inactivation of the Rps4 gene on the mouse X chromosomeA R Zinn, S L Bressler, P Beer-Romero, et al.
The British Journal of Dermatology|April 14, 2017
Evolution of the skin manifestations of X-linked pigmentary reticulate disorderP Starokadomskyy, L Sifuentes-Dominguez, T Gemelli, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 1998
Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouseM L Watson, A R Zinn, N Inoue, et al.
American Journal of Human Genetics|December 5, 1998
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1A R Zinn, V S Tonk, Z Chen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
Phenotypes Associated with SHOX DeficiencyJ L Ross, C Scott, P Marttila, et al.
Pageof 4