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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
Title:	Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290‐300.
Authors:	Clarke, CM¹, Fok, VT¹, Gustafson, JA¹, Smyth, MD^2,3, Timms, AE¹, Frazar, CD⁴, Smith, JD⁴, Birgfeld, CB^5,6,7, Lee, A^7,8,9, Ellenbogen, RG^7,8,9, Gruss, JS^5,6,7, Hopper, RA^5,6,7, Cunningham, ML^1,7,10, michael.cunningham@seattlechildrens.org
Source:	American Journal of Medical Genetics. Part A; Nov2018, Vol. 176 Issue 11, p2522-2522, 1p
Database:	Applied Science & Technology Source

Description
ISSN:	15524825
DOI:	10.1002/ajmg.a.38846