Holoprosencephaly as a genetic model for normal craniofacial development
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology
Cited by 58 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. Patterning of the antero‐ventral mammalian brain: Lessons from holoprosencephaly comparative biology in man and mouse;WIREs Mechanisms of Disease;2022-02-08
2. Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta;Taiwanese Journal of Obstetrics and Gynecology;2021-09
3. Novel heterozygous variants in KMT2D associated with holoprosencephaly;Clinical Genetics;2019-07-15
4. Semilobar holoprosencephaly with cebocephaly associated with maternal early onset preeclampsia: a case report;Journal of Medical Case Reports;2018-07-07
5. Further evidence for complex inheritance of holoprosencephaly: Lessons learned from pre‐ and postnatal diagnostic testing in Germany;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-06
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