Case report: a novel mutation in ZIC2 in an infant with microcephaly, holoprosencephaly, and arachnoid cyst
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference27 articles.
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2. Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans;Petryk;Wiley Interdiscip Rev Dev Biol,2015
3. Holoprosencephaly: clinical, anatomic, and molecular dimensions;Cohen;Birth Defects Res A Clin Mol Teratol,2006
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Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Semilobar Holoprosencephaly Caused by a Novel and De NovoZIC2Pathogenic Variant;Balkan Journal of Medical Genetics;2022-12-01
2. Familial and syndromic forms of arachnoid cyst implicate genetic factors in disease pathogenesis;Cerebral Cortex;2022-07-18
3. De novo ZIC2 frameshift variant associated with frontonasal dysplasia in a Limousin calf;BMC Genomics;2021-01-02
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