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Publications by Wolfgang Küster
Localization of the Gene Causing Keratolytic Winter Erythema to Chromosome 8p22-P23, and Evidence for a Founder Effect in South African Afrikaans-Speakers
American Journal of Human Genetics
Genetics
Related publications
Duplicated Enhancer Region Increases Expression of CTSB and Segregates With Keratolytic Winter Erythema in South African and Norwegian Families
American Journal of Human Genetics
Genetics
Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype
American Journal of Human Genetics
Genetics
Localization of a Gene for Progressive Myoclonus Epilepsy to Chromosome 21q22.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Localization of a Gene for Peripheral Arterial Occlusive Disease to Chromosome 1p31
American Journal of Human Genetics
Genetics
Growth Hormone Insensitivity With Immune Dysfunction Caused by a STAT5B Mutation in the South of Brazil: Evidence for a Founder Effect
Genetics and Molecular Biology
Genetics
Molecular Biology
Chromosome Localization of the Gene for Human Terminal Deoxynucleotidyltransferase to Region 10q23-Q25.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Founder Mutation inMYO7AUnderlies a Significant Proportion of Usher Syndrome in Indigenous South Africans: Implications for the African Diaspora
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Identification of a Common Founder Couple for 40 South African Afrikaner Families With Parkinson’s Disease
South African Medical Journal
Medicine
Localization of the Gene for Sclerosteosis to the Van Buchem Disease–Gene Region on Chromosome 17q12–q21
American Journal of Human Genetics
Genetics
