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PUBMED FOR HANDHELDS

Journal Abstract Search


176 related items for PubMed ID: 1539593

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  • 3. Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies.
    Wirth B, Voosen B, Röhrig D, Knapp M, Piechaczek B, Rudnik-Schöneborn S, Zerres K.
    Genomics; 1993 Jan; 15(1):113-8. PubMed ID: 8432521
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  • 5. Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3.
    Wirth B, Pick E, Leutner A, Dadze A, Voosen B, Knapp M, Piechaczek-Wappenschmidt B, Rudnik-Schöneborn S, Schönling J, Cox S.
    Genomics; 1994 Mar 01; 20(1):84-93. PubMed ID: 7912691
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  • 10. Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B.
    Soares VM, Brzustowicz LM, Kleyn PW, Knowles JA, Palmer DA, Asokan S, Penchaszadeh GK, Munsat TL, Gilliam TC.
    Genomics; 1993 Feb 01; 15(2):365-71. PubMed ID: 8449502
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  • 14. A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy.
    Yaraghi Z, McLean MD, Roy N, Surh L, Ikeda JE, Korneluk RG, MacKenzie A.
    Hum Genet; 1995 Sep 01; 96(3):330-4. PubMed ID: 7649551
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  • 16. Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy Investigators.
    Melki J, Sheth P, Abdelhak S, Burlet P, Bachelot MF, Lathrop MG, Frezal J, Munnich A.
    Lancet; 1990 Aug 04; 336(8710):271-3. PubMed ID: 1973971
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  • 17. Linkage analysis of spinal muscular atrophy.
    Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K.
    Genomics; 1992 Feb 04; 12(2):335-9. PubMed ID: 1346777
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  • 19. Microsatellite polymorphisms for chromosome 5 bands q11.2-q13.3.
    Sherrington R, Mankoo B, Dixon M, Curtis D, Kalsi G, Melmer G, Gurling H.
    Hum Hered; 1993 Feb 04; 43(3):197-202. PubMed ID: 8330884
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