Malformations of the craniofacial region: Evolutionary, embryonic, genetic, and clinical perspectives

被引：89

作者：

Cohen, MM ^{[1
]}

机构：

[1] Dalhousie Univ, Halifax, NS B3H 3J5, Canada

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 115卷 / 04期

关键词：

cnidarians; bilaterians; head organization genes; craniofacial genetics; craniofacial derivatives; neural crest; neurulation; multisited neural tube closure; anencephaly; meroacrania; holoacrania; encephalocele; holoprosencephaly; SHH; craniosynostosis; fibroblast growth factor receptors; TWIST; hypertelorism; branchial arch development; hernifacial microsomia; Treacher Collins syndrome; primary and secondary palate embryology; cleft lip; cleft palate; Robin sequence; Robin complexes;

D O I：

10.1002/ajmg.10982

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Malformations of the craniofacial region are reviewed with respect to evolutionary, embryonic, genetic, and clinical perspectives under the following headings: How Old Is Our Head?, Head Organization Genes, Genetics of Craniofacial Anomalies, Craniofacial Derivatives, Anencephaly, Cephalocele, Holoprosencephaly, Craniosynostosis, Hypertelorism, Branchial Arch Anomalies, and Orofacial Clefting. (C) 2002 Wiley-Liss, Inc.

引用

页码：245 / 268

页数：24

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