Caricamento...

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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Nicholls, R D, Gottlieb, W, Russell, L B, Davda, M, Horsthemke, B, Rinchik, E M
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1993
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC46018/
https://ncbi.nlm.nih.gov/pubmed/8095339
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !