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P Wieacker

Showing results (61-70 of 105) with videos related to

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Human Genetics|January 1, 1983
On the genetic length of the short arm of the human X chromosomeH H Ropers, P Wieacker, T F Wienker, et al.
Human Reproduction (Oxford, England)|June 29, 2012
Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndromeS Ledig, S Brucker, G Barresi, et al.
Acta Endocrinologica|February 1, 1993
Influence of steroid hormones on 5 alpha-reductase activity in female and male genital skin fibroblasts in cultureM W Beckmann, P Wieacker, M M Dereser, et al.
Cytogenetics and Cell Genetics|July 4, 2001
High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndromeM Stumm, S Neubauer, S Keindorff, et al.
Human Mutation|April 29, 1998
A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndromeT Dörk, F Schnieders, S Jakubiczka, et al.
Human Heredity|October 6, 2001
Preferential inactivation of a dupX(q23 --> q27-28) chromosome in a girl with mental retardation and dysmorphyM Volleth, M Stumm, K Mohnike, et al.
Fetal Diagnosis and Therapy|January 1, 1992
Pathophysiology of polyhydramnios in twin transfusion syndromeP Wieacker, C Wilhelm, H Prömpeler, et al.
Annales De Genetique|January 1, 1980
Assignment of the gene coding for human catalase to the short arm of chromosome 11P Wieacker, C R Mueller, A Mayerova, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 8, 2010
New technologies for the identification of novel genetic markers of disorders of sex development (DSD)A Bashamboo, S Ledig, P Wieacker, et al.
Human Genetics|January 1, 1983
Evidence that the Menkes locus maps on proximal XpT F Wienker, P Wieacker, H J Cooke, et al.
Pageof 11

Showing results (61-70 of 105) with videos related to

Sort By:
Pageof 11
Human Genetics|January 1, 1983
On the genetic length of the short arm of the human X chromosomeH H Ropers, P Wieacker, T F Wienker, et al.
Human Reproduction (Oxford, England)|June 29, 2012
Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndromeS Ledig, S Brucker, G Barresi, et al.
Acta Endocrinologica|February 1, 1993
Influence of steroid hormones on 5 alpha-reductase activity in female and male genital skin fibroblasts in cultureM W Beckmann, P Wieacker, M M Dereser, et al.
Cytogenetics and Cell Genetics|July 4, 2001
High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndromeM Stumm, S Neubauer, S Keindorff, et al.
Human Mutation|April 29, 1998
A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndromeT Dörk, F Schnieders, S Jakubiczka, et al.
Human Heredity|October 6, 2001
Preferential inactivation of a dupX(q23 --> q27-28) chromosome in a girl with mental retardation and dysmorphyM Volleth, M Stumm, K Mohnike, et al.
Fetal Diagnosis and Therapy|January 1, 1992
Pathophysiology of polyhydramnios in twin transfusion syndromeP Wieacker, C Wilhelm, H Prömpeler, et al.
Annales De Genetique|January 1, 1980
Assignment of the gene coding for human catalase to the short arm of chromosome 11P Wieacker, C R Mueller, A Mayerova, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 8, 2010
New technologies for the identification of novel genetic markers of disorders of sex development (DSD)A Bashamboo, S Ledig, P Wieacker, et al.
Human Genetics|January 1, 1983
Evidence that the Menkes locus maps on proximal XpT F Wienker, P Wieacker, H J Cooke, et al.
Pageof 11