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Ophthalmic Research|January 1, 1997
Molecular elucidation of hereditary eye diseases: pivotal role of the clinicianH H RopersEuropean Journal of Obstetrics, Gynecology, and Reproductive Biology|July 1, 1989
The recombinant DNA revolution: implications for diagnosis and prevention of inherited diseaseH H Ropers, B WieringaHuman Genetics|April 24, 1978
On the incidence of unilateral and bilateral colour blindness in heterozygous femalesK Feig, H H RopersHuman Genetics|April 17, 1979
Periodic hypokalemic paralysis transmitted by an unaffected male with negative family history: a delayed mutation?H H Ropers, H B SzliwowskiAmerican Journal of Medical Genetics|January 1, 1978
X-linked mental retardation: transmission of the trait by an apparently unaffected maleG Wolff, H Hameister, H H RopersClinical Genetics|February 1, 1977
Adrenoleukodystrophy (Siemerling-creutzfeldt disease): Heterozygote with two clonal fibroblast populationsH H Ropers, J Zimmermann, T WienkerClinical Genetics|September 1, 1985
X inactivation patterns in two syndromes with probable X-linked dominant, male lethal inheritanceP Wieacker, J Zimmer, H H RopersClinical Genetics|September 1, 1980
Addison disease and cerebral sclerosis in an apparently heterozygous girl: evidence for inactivation of the adrenoleukodystrophy locusW Heffungs, H Hameister, H H RopersClinical Genetics|July 1, 1982
Adrenoleukodystrophy: diagnosis and carrier detection by determination of long-chain fatty acids in cultured fibroblastsB Tönshoff, W Lehnert, H H RopersHuman Genetics|June 29, 1976
Fabry's disease: heterozygote detection by hair root analysisT Grimm, T F Wienker, H H RopersPageof 21