Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping-Reference-Cited by-同舟云学术

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Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping

Published:1999-01 Issue:1 Volume:64 Page:126-135
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Cormand Bru,Avela Kristiina,Pihko Helena,Santavuori Pirkko,Talim Beril,Topaloglu Haluk,de la Chapelle Albert,Lehesjoki Anna-Elina

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference48 articles.

1. Assignment of the mulibrey nanism gene to 17q by linkage analysis and allelic association;Avela;Am J Hum Genet,1997

2. β-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex;Bönnemann;Nat Genet,1995

3. Relationship between neuronal migration and cell-substratum adhesion: laminin and merosin promote olfactory neuronal migration but are anti-adhesive;Calof;J Cell Biol,1991

4. Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage;Campbell;Cell,1995

5. A metric map of humans: 23,500 loci in 850 bands;Collins;Proc Natl Acad Sci USA,1996

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