Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child-Reference-Cited by-同舟云学术

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Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child

Published:2015-07 Issue:3 Volume:16 Page:277-281
ISSN:1110-8630
Container-title:Egyptian Journal of Medical Human Genetics
language:en
Short-container-title:Egyptian Journal of Medical Human Genetics

Author:

Shawky Rabah M.,Gamal Radwa,Abdelsattar Mohammad Shaimaa

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference42 articles.

1. Neurological disorders. The mystery of the missing smile;Miller;Science,2007

2. HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1−/− mice;Webb;Am J Hum Genet,2012

3. Recent progress in understanding congenital cranial dysinnervation disorders;Oystreck;J Neuroophthalmol,2011

4. Mobius syndrome redefined: a syndrome of rhombencephalic maldevelopment;Verzijl;Neurology,2003

5. Living with Moebius syndrome: adjustment, social competence, and satisfaction with life;Bogart;Cleft Palate Craniofac J,2010

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