Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease

Tuberous sclerosis complex (TSC) is an autosomal dominant disorder of unknown aetiology that affects numerous body systems including skin, brain and kidneys. Some TSC has been linked to chromosome 9, additional TSC genes on chromosomes 11 and 12 have been proposed, but the majority of TSC families r...

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Veröffentlicht in:	Nature genetics 1992-09, Vol.2 (1), p.37-41
Hauptverfasser:	Kandt, R. S., Haines, J. L., Smith, M., Northrup, H., Gardner, R. J. M., Short, M. P., Dumars, K., Roach, E. S., Steingold, S., Wall, S., Blanton, S. H., Flodman, P., Kwiatkowski, D. J., Jewell, A., Weber, J. L., Roses, A. D., Pericak-Vance, M. A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Agriculture Alleles Animal Genetics and Genomics Biomedical and Life Sciences Biomedicine Cancer Research chromosome 16 Chromosomes, Human, Pair 16 Female Gene Function Genes, Dominant Genetic Linkage Genetic Markers Human Genetics Humans linkage analysis Lod Score Male man Pedigree polycystic kidney Polycystic Kidney, Autosomal Dominant - genetics tuberous sclerosis Tuberous Sclerosis - genetics
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