Assignment of a Form of Congenital Muscular Dystrophy with Secondary Merosin Deficiency to Chromosome 1q42-Reference-Cited by-同舟云学术

Assignment of a Form of Congenital Muscular Dystrophy with Secondary Merosin Deficiency to Chromosome 1q42

Published:2000-02 Issue:2 Volume:66 Page:428-435
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Brockington Martin,Sewry Caroline A.,Herrmann Ralf,Naom Isam,Dearlove Andrew,Rhodes Michael,Topaloglu Haluk,Dubowitz Victor,Voit Thomas,Muntoni Francesco

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference33 articles.

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4. Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping;Cormand;Am J Hum Genet,1999

5. Comprehensive genetic map of the human genome based on 5,264 microsatellites;Dib;Nature,1996

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