Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1-Reference-Cited by-同舟云学术

Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1

Published:2012-11-16 Issue:4 Volume:22 Page:696-703
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Slavotinek A. M.,Mehrotra P.,Nazarenko I.,Tang P. L.-F.,Lao R.,Cameron D.,Li B.,Chu C.,Chou C.,Marqueling A. L.,Yahyavi M.,Cordoro K.,Frieden I.,Glaser T.,Prescott T.,Morren M.-A.,Devriendt K.,Kwok P.-y.,Petkovich M.,Desnick R. J.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/22/4/696/13930516/dds477.pdf

Reference46 articles.

1. Setleis syndrome in Mexican-Nahua sibs due to a homozygous TWIST2 frameshift mutation and partial expression in heterozygotes: review of the focal facial dermal dysplasias and subtype reclassification

2. Preauricular Skin Defects

3. Focal preauricular dermal dysplasia: distinctive congenital lesions with a bilateral and symmetric distribution

4. Focal Preauricular Dermal Dysplasia: Report of Two Cases and a Review of Literature

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