Molecular screening ofSHH,ZIC2,SIX3, andTGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations-Reference-Cited by-同舟云学术

Molecular screening ofSHH,ZIC2,SIX3, andTGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations

Published:2004 Issue:1 Volume:24 Page:43-51
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Dubourg Christ�le,Lazaro Le�la,Pasquier Laurent,Bendavid Claude,Blayau Martine,Duff Franck Le,Durou Marie-Ren�e,Odent Sylvie,David V�ronique

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference34 articles.

1. Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations

2. Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

3. Expression of a novel murine homeobox gene in the developing cerebellar external granular layer during its proliferation

4. Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination

5. 2002. Possible association of NTDs with a polyhistidine tract polymorphism in the ZIC2 gene.

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