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Journal Abstract Search

227 related items for PubMed ID: 8852661

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  • 5. Duplications and de novo deletions of the SMNt gene demonstrated by fluorescence-based carrier testing for spinal muscular atrophy.
    Chen KL, Wang YL, Rennert H, Joshi I, Mills JK, Leonard DG, Wilson RB.
    Am J Med Genet; 1999 Aug 27; 85(5):463-9. PubMed ID: 10405443
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  • 7. Correlation between deletion patterns of SMN and NAIP genes and the clinical features of spinal muscular atrophy in Indian patients.
    Dastur RS, Gaitonde PS, Khadilkar SV, Udani VP, Nadkarni JJ.
    Neurol India; 2006 Sep 27; 54(3):255-9. PubMed ID: 16936383
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  • 10. Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents.
    Chang JG, Jong YJ, Lin SP, Soong BW, Tsai CH, Yang TY, Chang CP, Wang WS.
    Hum Genet; 1997 Oct 27; 100(5-6):577-81. PubMed ID: 9341874
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  • 11. Analysis of the SMN and NAIP genes in slovak spinal muscular atrophy patients.
    Zat'ková A, Hahnen E, Wirth B, Kádasi L.
    Hum Hered; 2000 Oct 27; 50(3):171-4. PubMed ID: 10686495
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  • 12. Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases.
    Cuscó I, Barceló MJ, del Rio E, Martín Y, Hernández-Chico C, Bussaglia E, Baiget M, Tizzano EF.
    Hum Genet; 2001 Mar 27; 108(3):222-9. PubMed ID: 11354634
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  • 13. Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes.
    Haider MZ, Moosa A, Dalal H, Habib Y, Reynold L.
    J Biomed Sci; 2001 Mar 27; 8(2):191-6. PubMed ID: 11287750
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  • 14. Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy.
    Al-Jumah M, Majumdar R, Al-Rajeh S, Awada A, Chaves-Carbello E, Salih M, Al-Shahwan S, Al-Subiey K, Al-Uthaim S.
    Saudi Med J; 2003 Oct 27; 24(10):1052-4. PubMed ID: 14578966
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  • 15. [A study of survival motor neuron and neuronal apoptosis inhibitory protein gene in spinal muscular atrophy].
    Zhang L, Yang X, Xiao B.
    Zhonghua Nei Ke Za Zhi; 2001 Jun 27; 40(6):401-4. PubMed ID: 11798607
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  • 16. Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients.
    Mrad R, Dorboz I, Ben Jemaa L, Maazoul F, Trabelsi M, Chaabouni M, Mlaiki B, Miladi N, Hentati F, Chaabouni H.
    Tunis Med; 2006 Aug 27; 84(8):465-9. PubMed ID: 17175684
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  • 17. Screening of deletions in SMN, NAIP and BTF2p44 genes in Turkish spinal muscular atrophy patients.
    Savas S, Gokgoz N, Kayserili H, Ozkinay F, Yuksel-Apak M, Kirdar B.
    Hum Hered; 2000 Aug 27; 50(3):162-5. PubMed ID: 10686493
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  • 19. Deletion of SMN and NAIP genes in Korean patients with spinal muscular atrophy.
    Shin S, Park SS, Hwang YS, Lee KW, Chung SG, Lee YJ, Park MH.
    J Korean Med Sci; 2000 Feb 27; 15(1):93-8. PubMed ID: 10719817
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  • 20. Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease.
    Moulard B, Salachas F, Chassande B, Briolotti V, Meininger V, Malafosse A, Camu W.
    Ann Neurol; 1998 May 27; 43(5):640-4. PubMed ID: 9585359
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