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P Wieacker

Showing results (11-20 of 105) with videos related to

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Human Genetics|April 4, 2008
Gene symbol: EFNB1. Disease: Craniofrontonasal syndromeIlse Wieland, P Wieacker, B Prager
Human Genetics|April 4, 2008
Gene symbol: EFNB1. Disease: Craniofrontonasal syndromeIlse Wieland, A Bohring, P Wieacker
Human Reproduction (Oxford, England)|August 1, 1989
Hirsutism, its pathogenesisM Breckwoldt, H P Zahradnik, P Wieacker
American Journal of Medical Genetics|September 1, 1987
Close linkage of the Wieacker-Wolff syndrome to the DNA segment DXYS1 in proximal XqP Wieacker, G Wolff, T F Wienker
Human Genetics|November 1, 1992
Point mutation in the steroid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndrome (CAIS)S Jakubiczka, E A Werder, P Wieacker
Clinical Genetics|September 1, 1985
X inactivation patterns in two syndromes with probable X-linked dominant, male lethal inheritanceP Wieacker, J Zimmer, H H Ropers
Cytogenetic and Genome Research|March 9, 2004
Multi-locus (ML)-FISH is a reliable tool for nondisjunction studies in human oocytesH Eckel, J Kleinstein, P Wieacker, et al.
Medizinische Klinik (Munich, Germany : 1983)|February 15, 1992
[Gonadotropin-releasing hormone (GnRH) and its analogs in current medicine]U Karck, J Neulen, P Wieacker, et al.
Geburtshilfe Und Frauenheilkunde|December 1, 1991
[Primary ovarian insufficiency in polyendocrinopathy syndrome]P Wieacker, D Emmerich, M Runge, et al.
Zeitschrift Fur Geburtshilfe Und Perinatologie|January 1, 1988
[Polyhydramnios in congenital myotonic dystrophy]P Wieacker, C Wilhelm, H Fürste, et al.
Pageof 11

Showing results (11-20 of 105) with videos related to

Sort By:
Pageof 11
Human Genetics|April 4, 2008
Gene symbol: EFNB1. Disease: Craniofrontonasal syndromeIlse Wieland, P Wieacker, B Prager
Human Genetics|April 4, 2008
Gene symbol: EFNB1. Disease: Craniofrontonasal syndromeIlse Wieland, A Bohring, P Wieacker
Human Reproduction (Oxford, England)|August 1, 1989
Hirsutism, its pathogenesisM Breckwoldt, H P Zahradnik, P Wieacker
American Journal of Medical Genetics|September 1, 1987
Close linkage of the Wieacker-Wolff syndrome to the DNA segment DXYS1 in proximal XqP Wieacker, G Wolff, T F Wienker
Human Genetics|November 1, 1992
Point mutation in the steroid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndrome (CAIS)S Jakubiczka, E A Werder, P Wieacker
Clinical Genetics|September 1, 1985
X inactivation patterns in two syndromes with probable X-linked dominant, male lethal inheritanceP Wieacker, J Zimmer, H H Ropers
Cytogenetic and Genome Research|March 9, 2004
Multi-locus (ML)-FISH is a reliable tool for nondisjunction studies in human oocytesH Eckel, J Kleinstein, P Wieacker, et al.
Medizinische Klinik (Munich, Germany : 1983)|February 15, 1992
[Gonadotropin-releasing hormone (GnRH) and its analogs in current medicine]U Karck, J Neulen, P Wieacker, et al.
Geburtshilfe Und Frauenheilkunde|December 1, 1991
[Primary ovarian insufficiency in polyendocrinopathy syndrome]P Wieacker, D Emmerich, M Runge, et al.
Zeitschrift Fur Geburtshilfe Und Perinatologie|January 1, 1988
[Polyhydramnios in congenital myotonic dystrophy]P Wieacker, C Wilhelm, H Fürste, et al.
Pageof 11