Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290‐300

Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290‐300

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Bibliographic Details
Published in:American journal of medical genetics. Part A Vol. 176; no. 11; p. 2522
Main Authors: Clarke, CM, Fok, VT, Gustafson, JA, Smyth, MD, Timms, AE, Frazar, CD, Smith, JD, Birgfeld, CB, Lee, A, Ellenbogen, RG, Gruss, JS, Hopper, RA, Cunningham, ML
Format: Journal Article
Language:English
Published: Hoboken, USA John Wiley & Sons, Inc 01-11-2018
Wiley Subscription Services, Inc
Subjects:
Craniosynostosis
Online Access:Get full text
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Bibliography:correction
ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.38846