Aberrant cell segregation in the craniofacial primordium and the emergence of facial dysmorphology in craniofrontonasal syndrome-Reference-Cited by-同舟云学术

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Aberrant cell segregation in the craniofacial primordium and the emergence of facial dysmorphology in craniofrontonasal syndrome

Published:2020-02-24 Issue:2 Volume:16 Page:e1008300
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Niethamer Terren K.^ORCID,Teng Teng^ORCID,Franco Melanie,Du Yu Xin,Percival Christopher J.^ORCID,Bush Jeffrey O.^ORCID

Funder

National Institute of Dental and Craniofacial Research

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics(clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference75 articles.

1. Global strategies to reduce the health care burden of craniofacial anomalies: report of WHO meetings on international collaborative research on craniofacial anomalies;W Shaw;Cleft Palate-Craniofacial J Off Publ Am Cleft Palate-Craniofacial Assoc,2004

2. New insights into craniofacial malformations;SRF Twigg;Hum Mol Genet,2015

3. Craniofrontonasal dysplasia;MM Cohen;Birth Defects Orig Artic Ser,1979

4. Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome;SRF Twigg;Proc Natl Acad Sci U S A,2004

5. Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome;I Wieland;Am J Hum Genet,2004

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