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PUBMED FOR HANDHELDS

Journal Abstract Search

122 related items for PubMed ID: 7874111

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  • 23. Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.
    DiDonato CJ, Morgan K, Carpten JD, Fuerst P, Ingraham SE, Prescott G, McPherson JD, Wirth B, Zerres K, Hurko O.
    Am J Hum Genet; 1994 Dec; 55(6):1218-29. PubMed ID: 7977383
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  • 26. Isolation of microsatellites from the spinal muscular atrophy (SMA) candidate region on chromosome 5q and linkage analysis in Spanish SMA families.
    Velasco E, Valero C, García E, de la Puente A, Cruces J, San Millán JL, del Castillo I, Coloma A, Moreno F, Hernández-Chico C.
    Eur J Hum Genet; 1995 Dec; 3(2):96-101. PubMed ID: 7552147
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  • 28. An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA).
    Helmken C, Wetter A, Rudnik-Schöneborn S, Liehr T, Zerres K, Wirth B.
    Eur J Hum Genet; 2000 Jul; 8(7):493-9. PubMed ID: 10909848
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  • 31. Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markers.
    Clermont O, Burlet P, Burglen L, Lefebvre S, Pascal F, McPherson J, Wasmuth JJ, Cohen D, Le Paslier D, Weissenbach J.
    Am J Hum Genet; 1994 Apr; 54(4):687-94. PubMed ID: 8128967
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  • 32. A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysis.
    van der Steege G, Cobben JM, Osinga J, Scheffer H, van Ommen GJ, Buys CH.
    Hum Genet; 1995 Nov; 96(5):589-91. PubMed ID: 8530008
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  • 33. 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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  • 37. Programmed cell death and the gene behind spinal muscular atrophy.
    Robinson A.
    CMAJ; 1995 Nov 15; 153(10):1459-62. PubMed ID: 7585374
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  • 40. An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.
    Mérette C, Brzustowicz LM, Daniels RJ, Davies KE, Gilliam TC, Melki J, Munnich A, Pericak-Vance MA, Siddique T, Voosen B.
    Genomics; 1994 May 01; 21(1):27-33. PubMed ID: 8088801
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