Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly.

Lissencephaly (agyria-pachygyria) is a brain malformation manifested by a smooth cerebral surface, resulting from arrest of neuronal migration at 10-14 wk gestation. Type I, or classical, lissencephaly can occur either in association with the Miller-Dieker syndrome (MDS) or as an isolated finding, t...

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Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Ledbetter, S A, Kuwano, A, Dobyns, W B, Ledbetter, D H
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1992
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682541/
https://ncbi.nlm.nih.gov/pubmed/1346078
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