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Human Genetics|February 1, 1980
The presence of androgen-binding receptors in genital and nongenital skin fibroblastsJ Herfert, T F Wienker, H H RopersHuman Genetics|September 19, 1978
Preferential X inactivation in human placenta membranes: is the paternal X inactive in early embryonic development of female mammals?H H Ropers, G Wolff, H W HitzerothHuman Genetics|January 1, 1982
Flow cytometric characterization of a Chinese hamster X man hybrid cell line retaining the human Y chromosomeC Cremer, J W Gray, H H RopersClinical Genetics|June 1, 1976
Prenatal diagnosis of homoxygous familial hypercholesterolemia: investigation of a case at riskT F Wienker, G Utermann, H H RopersActa Anthropogenetica|January 1, 1983
Exclusion of the C3 gene from the 19q133 to 19qter region by Southern analysis of human-rodent somatic cell hybrids, employing a cloned genomic C3 gene fragmentP Wieacker, G Fey, I Voiculescu, et al.Human Genetics|January 1, 1982
Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocationH H Ropers, O Zuffardi, E Bianchi, et al.Human Genetics|May 23, 1979
Progressive myoclonus epilepsy. A variant with probable X-linked inheritanceT F Wienker, G M von Reutern, H H RopersAmerican Journal of Human Genetics|July 1, 1975
Leukodystrophy, skin hyperpigmentation, and adrenal atrophy: Siemerling-Creutzfeldt disease. Transmission through several generations in two familiesH H Ropers, P Burmeister, W v Petrykowski, et al.The British Journal of Dermatology|December 1, 1981
X-linked recessive ichthyosis in three sisters: evidence for homozygosityB Mevorah, E Frenk, C R Müller, et al.Human Genetics|January 1, 1980
X-linked steroid sulfatase: evidence for different gene-dosage in males and femalesC R Müller, B Migl, H Traupe, et al.Pageof 21