Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype-Reference-Cited by-同舟云学术

Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype

Published:2010-12-28 Issue:1 Volume:155 Page:207-214
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Abdel-Salam Ghada M. H.,Flores-Sarnat Laura,El-Ruby Mona O.,Parboosingh Jillian,Bridge Peter,Eid Maha M.,El-Badry Tarek H.,Effat Laila,Curatolo Paolo,Temtamy Samia A.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33777/fullpdf

Reference28 articles.

1. Craniofacial dyssynostosis with cryptorchidism and normal stature;Al-Torki;Am J Med Genet,1998

2. Muenke syndrome with osteochondroma;Barbosa;Am J Med Genet Part A,2009

3. Deletion of 15q11.2-15q13.1 in isolated human hemimegalencephaly;Baybis;Acta Neuropathol,2009

4. Craniofacial dyssynostosis: Description of the first four Spanish cases and review;Bermejo;Am J Med Genet Part A,2005

5. Cerebellum-small brain but large confusion: A review of selected cerebellar malformations and disruptions;Boltshauser;Am J Med Genet Part A,2004

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