Camptodactyly and the 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Camptodactyly and the 22q11.2 deletion syndrome

Published:2016-10-28 Issue:2 Volume:173 Page:515-518
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Couser Natario L.¹²,Pande Chetna K.³⁴,Walsh Jonathan M.⁵⁶,Tepperberg James⁷,Aylsworth Arthur S.¹⁸

Affiliation:

1. Department of Pediatrics; Division of Genetics and Metabolism; School of Medicine; University; of North Carolina at Chapel Hill; Chapel Hill North Carolina

2. Department of Ophthalmology; University of North Carolina at Chapel Hill; Chapel Hill North Carolina

3. Texas Tech Health Sciences Center; Paul L. Foster School of Medicine; El Paso Texas

4. Department of Pediatrics; Johns Hopkins University School of Medicine; Baltimore Maryland

5. Department of Otolaryngology/Head and Neck Surgery; University of North Carolina at Chapel Hill; Chapel Hill North Carolina

6. Department of Otolaryngology/Head and Neck Surgery; Johns Hopkins University School of Medicine; Baltimore Maryland

7. LabCorp; Research Triangle Park; North Carolina

8. Department of Genetics; University of North Carolina at Chapel Hill; Chapel Hill North Carolina

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.38029/fullpdf

Reference26 articles.

1. The neurocognitive phenotype in velo-cardio-facial syndrome: A developmental perspective;Antshel;Dev Disabil Res Rev,2008

2. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;J Pediatr,2011

3. Camptodactyly: Classification and results of nonoperative treatment;Benson;J Pediatr Orthop,1994

4. Elements of morphology: Standard terminology for the hands and feet;Biesecker;Am J Med Genet Part A,2009

5. Congenital glottic webs in children. A retrospective review of 51 patients;Cohen;Ann Otol Rhinol Laryngol Suppl,1985

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5. Camptodactyly and the 22q11.2 deletion syndrome;American Journal of Medical Genetics Part A;2016-10-28