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Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
by
Hillaire, Dominique
,
Leclerc, Anne
,
Fauré, Sabine
,
Topaloglu, Haluk
,
Chiannllkulchaï, Nuchanard
,
Guicheney, Pascale
,
Grinas, Laurent
,
Legos, Patricia
,
Philpot, Joanne
,
Evangelista, Teresinha
,
Routon, Marie-Claude
,
Mayer, Michèle
,
Pellissier, Jean-Francols
,
Estournet, Brigitte
,
Barols, Annie
,
Hentati, Fayçal
,
Feingold, Nicole
,
S.Beckmann, Jacqui
,
Dubowitz, Victor
,
M.S.Tomé, Fernando
,
Fardeau, Michel
Published in
Human molecular genetics
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Hum Mol Genet
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Human Molecular Genetics
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Biochemistry & Molecular Biology
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Biological And Medical Sciences
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Chromosome 6
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Chromosome Mapping
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Chromosomes, Human, Pair 6
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Chromosomes, Human, Pair 9
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Consanguinity
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Diseases Of Striated Muscles. Neuromuscular Diseases
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Female
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Fukuyama Type
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Genetic Linkage
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Genetic Markers
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Genetics & Heredity
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Homozygote
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Humans
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Laminin - Deficiency
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Laminin - Genetics
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Life Sciences & Biomedicine
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Male
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Oxford University Press:jisc Collections:oxford Journal Archive: Access Period 2024-2025
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