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Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families.

We have used three highly polymorphic microsatellite repeats from Xq21 to type families in whom a gene for X linked deafness with perilymphatic gusher (DFN 3) was segregating. All three markers were tightly linked to the disease in its radiologically normal and abnormal forms, with a maximum lod sco...

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Detalhes bibliográficos
Main Authors: Bitner-Glindzicz, M, de Kok, Y, Summers, D, Huber, I, Cremers, F P, Ropers, H H, Reardon, W, Pembrey, M E, Malcolm, S
Formato: Artigo
Idioma:Inglês
Publicado em: 1994
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016689/
https://ncbi.nlm.nih.gov/pubmed/7891371
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