Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.

Prader-Willi and Angelman syndromes are complex neurobehavioral contiguous gene syndromes whose expression depends on the unmasking of genomic imprinting for different genetic loci in human chromosome 15q11-q13. The homologous chromosomal region in the mouse genome has been fine-mapped by using inte...

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Publicado en:	Proc Natl Acad Sci U S A
Autores principales:	Nicholls, R D, Gottlieb, W, Russell, L B, Davda, M, Horsthemke, B, Rinchik, E M
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	National Academy of Sciences 1993
Materias:	Research Article
Acceso en línea:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC46018/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8095339/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.90.5.2050
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