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Molecular Biopsy of Human Tumors

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  • 21. High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy.
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    Tay J
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  • 23. [DNA diagnosis of Duchenne muscular dystrophy].
    Matsumoto T
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    Uchida T; Ogata H; Shirai Z; Mitsudome A
    No To Hattatsu; 1988 Jan; 20(1):28-32. PubMed ID: 3279979
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    Neurol Neurochir Pol; 1993; 27(4):469-78. PubMed ID: 8247234
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    Claustres M; Kjellberg P; Desgeorges M; Bellet H; Sarda P; Bonnet H; Boileau C
    J Genet Hum; 1989 Sep; 37(3):251-7. PubMed ID: 2625628
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    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(8):29-33. PubMed ID: 2175114
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    [No Abstract]   [Full Text] [Related]  

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    Hausmanowa-Petrusewicz I; Borkowska J
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    [No Abstract]   [Full Text] [Related]  

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    Kondo K; Tsubaki T
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