Holoprosencephaly, telecanthus and ectrodactyly-Reference-Cited by-同舟云学术

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Holoprosencephaly, telecanthus and ectrodactyly

Published:1992-01 Issue:1 Volume:1 Page:47???52
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:Clinical Dysmorphology

Author:

YOUNG I. D.,ZUCCOLLO J. M.,BARROW M.,FOWLIE A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Cited by 13 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. Novel heterozygous mutation in the extracellular domain of FGFR1 associated with Hartsfield syndrome;Human Genome Variation;2016-10-13

2. Novel de novo heterozygousFGFR1mutation in two siblings with Hartsfield syndrome: A case of gonadal mosaicism;American Journal of Medical Genetics Part A;2014-05-28

3. Microduplication of Xq24 and Hartsfield syndrome with holoprosencephaly, ectrodactyly, and clefting;American Journal of Medical Genetics Part A;2012-08-10

4. Holoprosencephaly in an Egyptian baby with ectrodactyly-ectodermal dysplasia-cleft syndrome: a case report;Journal of Medical Case Reports;2012-01-24

5. Maternal Serum Screening for Neural Tube and Other Defects;Genetic Disorders and the Fetus;2010-09-24

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