Muenke syndrome (FGFR3-related craniosynostosis): Expansion of the phenotype and review of the literature-Reference-Cited by-同舟云学术

Muenke syndrome (FGFR3-related craniosynostosis): Expansion of the phenotype and review of the literature

Published:2007 Issue:24 Volume:143A Page:3204-3215
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Doherty Emily S.,Lacbawan Felicitas,Hadley Donald W.,Brewer Carmen,Zalewski Christopher,Kim H. Jeff,Solomon Beth,Rosenbaum Kenneth,Domingo Demetrio L.,Hart Thomas C.,Brooks Brian P.,Immken LaDonna,Lowry R. Brian,Kimonis Virginia,Shanske Alan L.,Jehee Fernanda Sarquis,Bueno Maria Rita Passos,Knightly Carol,McDonald-McGinn Donna,Zackai Elaine H.,Muenke Maximilian

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32078/fullpdf

Reference49 articles.

1. Jackson-Weiss syndrome: Clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qter

2. Postoperative Mental and Morphological Outcome for Nonsyndromic Brachycephaly

3. Speech, Cognitive, and Behavioral Outcomes in Nonsyndromic Craniosynostosis

4. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

5. No association betweenDFNA6 and Pro250Arg mutation inFGFR3

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