Point Mutations and an Intragenic Deletion in LIS1, the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome-Reference-Cited by-同舟云学术

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Point Mutations and an Intragenic Deletion in LIS1, the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome

Published:1997-02-01 Issue:2 Volume:6 Page:157-164
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Lo Nigro C.,Chong S. S.,Smith A. C. M.,Dobyns W. B.,Carrozzo R.,Ledbetter D. H.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference28 articles.

1. The spectrum of lissencephaly: Report of ten patients analyzed by magnetic resonance imaging

2. Causal heterogeneity in isolated lissencephaly

3. Lissencephaly and Other Malformations of Cortical Development: 1995 Update

4. X-linked malformations of neuronal migration

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