Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.

Angelman syndrome (AS) and Prader-Willi syndrome (PWS) share a cytogenetic deletion of chromosome 15q11q13. To determine the extent of deletion in AS we analyzed the DNA of 19 AS patients, including two sib pairs, with the following chromosome 15q11q13--specific DNA markers: D15S9-D15S13, D15S17, D1...

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Autori principali: Knoll, J H, Nicholls, R D, Magenis, R E, Glatt, K, Graham, J M, Kaplan, L, Lalande, M
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1990
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683759/
https://ncbi.nlm.nih.gov/pubmed/1971993
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