The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.

The KE family is a large three-generation pedigree in which half the members are affected with a severe speech and language disorder that is transmitted as an autosomal dominant monogenic trait. In previously published work, we localized the gene responsible (SPCH1) to a 5.6-cM region of 7q31 betwee...

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Detaylı Bibliyografya
Asıl Yazarlar: Lai, C, Fisher, S, Hurst, J, Levy, E, Hodgson, S, Fox, M, Jeremiah, S, Povey, S, Jamison, D, Green, E, Vargha-Khadem, F, Monaco, A
Materyal Türü: Journal article
Dil:English
Baskı/Yayın Bilgisi: 2000

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