Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population
Baldwin, C T, Weiss, S, Farrer, L A, De Stefano, A L, Adair, R, Franklyn, B, Kidd, K K, Korostishevsky, M, Bonné-Tamir, B
Published in Human molecular genetics (01.09.1995)
Published in Human molecular genetics (01.09.1995)
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Journal Article
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease
Iyengar, S, Kalinsky, H, Weiss, S, Korostishevsky, M, Sadeh, M, Zhao, Y, Kidd, K K, Bonne-Tamir, B
Published in Journal of medical genetics (01.05.1997)
Published in Journal of medical genetics (01.05.1997)
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