X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): Clinical, magnetic resonance imaging, and neuropathological findings-Reference-Cited by-同舟云学术

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): Clinical, magnetic resonance imaging, and neuropathological findings

Published:2002-02-27 Issue:3 Volume:51 Page:340-349
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Bonneau Dominique,Toutain Annick,Laquerrière Annie,Marret Stéphane,Saugier-Veber Pascale,Barthez Marie-Anne,Radi Sophie,Biran-Mucignat Valérie,Rodriguez Diana,Gélot Antoinette

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference12 articles.

1. Lissencephaly and other malformations of cortical development: 1995 update;Dobyns;Neuropediatrics,1995

2. Dobyns WB http://www.geneclinics.org.

3. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation;Pilz;Hum Mol Genet,1998

4. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome;des Portes;Cell,1998

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