Polydactyly in a carrier of the gene for the meckel syndrome-Reference-Cited by-同舟云学术

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Polydactyly in a carrier of the gene for the meckel syndrome

Published:1994-11-15 Issue:3 Volume:53 Page:207-209
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Nelson John,Nevin Norman C.,Hanna E. Jennifer

Publisher

Wiley

Subject

Genetics (clinical)

Reference10 articles.

1. The Meckel syndrome with limited expression in relatives

2. Spectrum of anomalies in the Meckel syndrome, or: “Maybe there is a malformation syndrome with at least one constant anomaly”

3. Variability in the Smith-Lemli-Opitz syndrome: Overlap with the meckel syndrome

4. Survival and spectrum of anomalies in the meckel syndrome

Cited by 6 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. Syndrome de Meckel Gruber: à propos d’un cas rare;Pan African Medical Journal;2016

2. Bartsocas-Papas Syndrome: Unusual Findings in the First Reported Egyptian Family;Case Reports in Genetics;2011

3. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

4. Síndrome de Meckel-Gruber;Clínica e Investigación en Ginecología y Obstetricia;2001-01

5. Meckel syndrome.;Journal of Medical Genetics;1998-06-01

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