Associated malformations in the family of a patient with Meckel syndrome: heterozygous expression?-Reference-Cited by-同舟云学术

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Associated malformations in the family of a patient with Meckel syndrome: heterozygous expression?

Published:1997-11-01 Issue:11 Volume:34 Page:937-938
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Gulati R,Phadke S R,Agarwal S S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference5 articles.

1. Meckel syndrome;Johnson, V.P.,1990

2. Genetics of the Meckel syndrome (dysencephalia splanchnocystica);Hsia, Y.E.; Bratu, M.; Herbordt, A.;Pediatrics,1971

3. Features of the 13-15 trisomy syndrome with normal karyotype;Marshall, R.; Newnham, R.E.; Rawstron, JR;Lancet,1964

4. The Meckel syndrome with limited expression in relatives;Fitch, N.; Pinsky, L.;Clin Genet,1973

5. The locus for Meckel syndrome maps to chromosome with multiple congenital anomalies 17q21-q24;Paavola, P.; Salonen, R.; Weissenbach, J.; Peltonen, L.,1995

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. Fetal Autopsy of Meckel Gruber Syndrome –A Case Report;Fetal and Pediatric Pathology;2013-02-27

2. Mental retardation, short stature and synpolydactyly in a manifesting heterozygote of Bartsocas-Papas syndrome;Clinical Genetics;2012-12-21

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

4. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003

5. Lexikon der Syndrome und Fehlbildungen;Lexikon der Syndrome und Fehlbildungen;1999

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