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PubMed · 1886791

A new polymorphic probe on chromosome 3p: lambda LIB36-68 (D3S615).

L Geil·F Latif·M Yao·M L Orcutt·B Zbar·M I Lerman
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Chromosomes, Human, Pair 3DNA ProbesDeoxyribonucleases, Type II Site-SpecificHumansPolymorphism, GeneticWhite Peoplevon Hippel-Lindau DiseaseJournal ArticleResearch Support, U.S. Gov't, P.H.S.

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L Geil, F Latif, M Yao, M L Orcutt, B Zbar, M I Lerman. 1991-08-25. A new polymorphic probe on chromosome 3p: lambda LIB36-68 (D3S615).. https://doi.org/10.1093/nar%2F19.16.4569

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Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British origin.

Linkage analysis has been performed on a large South African family of British origin in which 39 persons in 6 generations had early onset Type I autosomal dominant retinitis pigmentosa (ADRP). Tight linkage was excluded between the disease and the D3S47 locus on chromosome 3. This finding is further evidence for genetic heterogeneity in ADRP.

Chromosomes, Human, Pair 3↗