A Gene for Meckel Syndrome Maps to Chromosome 11q13-Reference-Cited by-同舟云学术

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A Gene for Meckel Syndrome Maps to Chromosome 11q13

Published:1998-10 Issue:4 Volume:63 Page:1095-1101
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Roume J.,Genin E.,Cormier-Daire V.,Ma H.W.,Mehaye B.,Attie T.,Razavi-Encha F.,Fallet-Bianco C.,Buenerd A.,Clerget-Darpoux F.,Munnich A.,Le Merrer M.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. A distinctive triad malformations of the central nervous system in the Meckel-Grüber syndrome;Ahdab-Barmada;J Neuropathol Exp Neurol,1990

2. Cerebellocele and associated central nervous system anomalies in the Meckel syndrome;Aleksic;Childs Brain,1984

3. Pathology of renal and hepatic anomalies in Meckel syndrome;Blankenberg;Am J Med Genet Suppl,1987

4. Meckel's syndrome (dysencephalia slanchnocystica) in two Pakistani sibs;Crawford;J Med Genet,1978

5. A comprehensive genetic map of the human genome based on 5264 microsatellites;Dib;Nature,1996

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