A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.

The genetic defects in Prader-Willi syndrome (PWS) and Angelman syndrome (AS) map to 15q11-13. Using microdissection, we have recently isolated several DNA probes for the critical region. Here we report that microclone MN7 detects multiple loci in 15q11-13 and 16p11.2. Eight yeast artificial chromos...

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Main Authors: Buiting, K, Greger, V, Brownstein, B H, Mohr, R M, Voiculescu, I, Winterpacht, A, Zabel, B, Horsthemke, B
Formato: Artigo
Idioma:Inglês
Publicado: 1992
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC49311/
https://ncbi.nlm.nih.gov/pubmed/1608955
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