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P Wieacker

Showing results (71-80 of 105) with videos related to

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Human Genetics|January 1, 1983
Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphismP Wieacker, N Horn, P Pearson, et al.
Cytogenetic and Genome Research|August 6, 2003
Mapping of a further locus for X-linked craniofrontonasal syndromeI Wieland, S Jakubiczka, P Muschke, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Female pseudohermaphroditism caused by caudal dysgenesisP Wieacker, U Grumpelt, T Schulz, et al.
Human Molecular Genetics|May 16, 1998
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoformsB Klamt, A Koziell, F Poulat, et al.
Journal of Medical Genetics|February 12, 2002
Partial trisomy 9p12p21.3 with a normal phenotypeM Stumm, J Müsebeck, H Tönnies, et al.
Human Genetics|January 1, 1985
X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosomeU Friedrich, M Warburg, P Wieacker, et al.
American Journal of Medical Genetics|December 18, 1998
Familial occurrence of a del(Xp-) chromosome: pitfall in karyotype/phenotype correlationA Soyke, M Stumm, P Krebs, et al.
Human Molecular Genetics|September 25, 1997
Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmiasB Wollnik, B C Schroeder, C Kubisch, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 15, 2010
Mutations of the SRY-responsive enhancer of SOX9 are uncommon in XY gonadal dysgenesisI Georg, S Bagheri-Fam, K C Knower, et al.
Human Genetics|July 1, 1987
Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segmentP Wieacker, J E Griffin, T Wienker, et al.
Pageof 11

Showing results (71-80 of 105) with videos related to

Sort By:
Pageof 11
Human Genetics|January 1, 1983
Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphismP Wieacker, N Horn, P Pearson, et al.
Cytogenetic and Genome Research|August 6, 2003
Mapping of a further locus for X-linked craniofrontonasal syndromeI Wieland, S Jakubiczka, P Muschke, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Female pseudohermaphroditism caused by caudal dysgenesisP Wieacker, U Grumpelt, T Schulz, et al.
Human Molecular Genetics|May 16, 1998
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoformsB Klamt, A Koziell, F Poulat, et al.
Journal of Medical Genetics|February 12, 2002
Partial trisomy 9p12p21.3 with a normal phenotypeM Stumm, J Müsebeck, H Tönnies, et al.
Human Genetics|January 1, 1985
X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosomeU Friedrich, M Warburg, P Wieacker, et al.
American Journal of Medical Genetics|December 18, 1998
Familial occurrence of a del(Xp-) chromosome: pitfall in karyotype/phenotype correlationA Soyke, M Stumm, P Krebs, et al.
Human Molecular Genetics|September 25, 1997
Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmiasB Wollnik, B C Schroeder, C Kubisch, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 15, 2010
Mutations of the SRY-responsive enhancer of SOX9 are uncommon in XY gonadal dysgenesisI Georg, S Bagheri-Fam, K C Knower, et al.
Human Genetics|July 1, 1987
Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segmentP Wieacker, J E Griffin, T Wienker, et al.
Pageof 11