Muenke syndrome: An international multicenter natural history study-Reference-Cited by-同舟云学术

Muenke syndrome: An international multicenter natural history study

Published:2016-01-06 Issue:4 Volume:170 Page:918-929
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kruszka Paul¹,Addissie Yonit A.¹,Yarnell Colin M. P.¹,Hadley Donald W.¹,Guillen Sacoto Maria J.¹,Platte Petra²,Paelecke Yvonne²,Collmann Hartmut³,Snow Nicole⁴⁵,Schweitzer Tilmann³,Boyadjiev Simeon A.⁶,Aravidis Christos⁷,Hall Samantha E.⁸,Mulliken John B.⁸,Roscioli Tony³⁴,Muenke Maximilian¹

Affiliation:

1. Medical Genetics Branch; National Human Genome Research Institute; The National Institutes of Health; Bethesda Maryland

2. Department of Biological Psychology; Clinical Psychology and Psychotherapy; University of Würzburg; Germany

3. Section of Pediatric Neurosurgery; Department of Neurosurgery; University of Würzburg; Germany

4. Sydney Children's Hospital; University of New South Wales; Sydney Australia

5. Kinghorn Centre for Clinical Genomics; The Garvan Institute; Darlinghurst Sydney Australia

6. Department of Pediatrics; Section of Genetics; University of California Davis; Sacramento California

7. Department of Clinical Genetics; Akademiska University Hospital; Uppsala Sweden

8. Department of Plastic and Oral Surgery; Boston Children's Hospital; Boston Massachusetts

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37528/fullpdf

Reference35 articles.

1. Hearing loss in syndromic craniosynostoses: Introduction and consideration of mechanisms;Agochukwu;Am J Audiol,2014

2. Postoperative mental and morphological outcome for nonsyndromic brachycephaly;Arnaud;Plast Reconstr Surg,2002

3. Health-related quality of life in children and adolescents with syndromic craniosynostosis;Bannink;J Plast Reconstr Aesthet Surg,2010

4. Obstructive sleep apnea-specific quality of life and behavioral problems in children with syndromic craniosynostosis;Bannink;J Dev Behav Pediatr,2011

5. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes;Bellus;Nat Genet,1996

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