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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
Author(s) -
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
Publication year - 2018
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.38846
Subject(s) - proband , genetics , table (database) , craniosynostosis , identification (biology) , medicine , biology , gene , computer science , mutation , data mining , botany
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