Rare ACTG1 variants in fetal microlissencephaly-Reference-Cited by-同舟云学术

Rare ACTG1 variants in fetal microlissencephaly

Published:2015-08 Issue:8 Volume:58 Page:416-418
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Poirier Karine,Martinovic Jelena,Laquerrière Annie,Cavallin Mara,Fallet-Bianco Catherine,Desguerre Isabelle,Valence Stephanie,Grande-Goburghun Jocelyne,Francannet Christine,Deleuze Jean-François,Boland Anne,Chelly Jamel,Bahi-Buisson Nadia

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference7 articles.

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2. Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly;Dobyns;Am. J. Med. Genet.,1984

3. Severe forms of Baraitser-Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations;Di Donato;Eur. J. Hum. Genet. EJHG,2014

4. Organ weights in human fetuses after formalin fixation: standards by gestational age and body weight;Guihard-Costa;Pediatr. Dev. Pathol. Off. J. Soc. Pediatr. Pathol. Paediatr. Pathol. Soc.,2002

5. Lissencephaly;Norman;Can. J. Neurol. Sci.,1976

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