Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

The X linked form of Kallmann syndrome (KAL) and X linked ocular albinism (OA1) have both been mapped to Xp22.3. We have used a dinucleotide repeat polymorphism at the Kallmann locus to type 17 X linked ocular albinism families which had previously been typed for the Xg blood group (XG) and the DNA...

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Detalhes bibliográficos

Publicado no:	J Med Genet
Principais autores:	Zhang, Y, McMahon, R, Charles, S J, Green, J S, Moore, A T, Barton, D E, Yates, J R
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMJ Publishing Group 1993
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016600/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8301646/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.11.923
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