Molecular screening for proximal 15q abnormalities in a mentally retarded population.

Paternal or maternal deletions in the 15q11.2-q13 region are known to result in Prader-Willi syndrome (PWS) or Angelman syndrome (AS), respectively. Maternal duplications in 15q11.2-q13 have been found in patients with autism. A population of adults with moderate to profound mental retardation was s...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Jacobsen, J, King, B H, Leventhal, B L, Christian, S L, Ledbetter, D H, Cook, E H
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1998
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051362/
https://ncbi.nlm.nih.gov/pubmed/9678696
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