Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype
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Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype
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External Links
(P356) |
10.1002/1531-8249(199906)45:6<751::AID-ANA9>3.0.CO;2-M
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(P698) |
10360767
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