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Compound heterozygosity in a South African patient with Facioscapulohumeral muscular dystrophy
by
Olckers, Antonel
,
van der Merwe, Annelize
,
Wayne Towers, G
,
Retief, Chris F
,
Honey, Engela
,
Schutte, Clara-Maria
Published in
Neuromuscular disorders : NMD
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Journal Title
Neuromuscular Disorders : Nmd
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Subjects
Chromosomes, Human, Pair 4 - Genetics
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Clinical Neurology
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Compound Heterozygote
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Deoxyribonuclease Ecori - Genetics
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Deoxyribonucleases, Type Ii Site-Specific - Genetics
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Facioscapulohumeral Muscular Dystrophy
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Fshd
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Gene Deletion
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Genotype-Phenotype Correlation
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Genotype–Phenotype Correlation
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Haplotypes - Genetics
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Heterozygote
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Humans
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Life Sciences & Biomedicine
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Male
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Middle Aged
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Muscular Dystrophy
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Muscular Dystrophy, Facioscapulohumeral - Ethnology
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Muscular Dystrophy, Facioscapulohumeral - Genetics
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Neurology
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Sciencedirect®
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Elsevier
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