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Exclusion of mutations in TGIF , ALX3 , and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies
Author(s) -
RibeiroBicudo Lucilene Arilho,
Quiezi Rodrigo G.,
GuionAlmeida Maria Leine,
Legnaro Chiara,
RichieriCosta Antonio
Publication year - 2012
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.35305
Subject(s) - craniofacial , medicine , agenesis , dental anomalies , medical genetics , dysgenesis , pediatrics , anatomy , genetics , biology , dentistry , psychiatry , gene
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