Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly-Reference-Cited by-同舟云学术

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Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

Published:1989-10 Issue:2 Volume:34 Page:237-245
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Münke Maximilian

Publisher

Wiley

Subject

Genetics(clinical)

Reference125 articles.

1. Cyclopia and Maternal Ingestion of Salicylates

2. Holoprosencephaly in infants of diabetic mothers

Cited by 89 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. Genetic Syndromes of Hypothalamic Dysfunction;The Human Hypothalamus;2020-12-25

2. 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

3. Cyclopia-otocephaly-agnathia-synotia-astomia complex: A case report;Journal of Clinical Neonatology;2018

4. Prosencephalic Development;Volpe's Neurology of the Newborn;2018

5. Holoprosencephaly;Atlas of Genetic Diagnosis and Counseling;2017

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