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Journal Abstract Search

144 related items for PubMed ID: 10206524

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  • 3. 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; 54(3):255-9. PubMed ID: 16936383
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  • 6. SMN(T) and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): genotype/phenotype correlations with disease severity.
    Simard LR, Rochette C, Semionov A, Morgan K, Vanasse M.
    Am J Med Genet; 1997 Oct 03; 72(1):51-8. PubMed ID: 9295075
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  • 7. 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 03; 15(1):93-8. PubMed ID: 10719817
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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 03; 100(5-6):577-81. PubMed ID: 9341874
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  • 13. [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 03; 40(6):401-4. PubMed ID: 11798607
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  • 14. Prenatal diagnosis of spinal muscular atrophy in Turkish families.
    Erdem H, Dayangaç D, Pehlivan S, Topaloglu H.
    Cent Eur J Public Health; 2001 Feb 03; 9(1):35-7. PubMed ID: 11243588
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  • 17. Study of survival of motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) gene deletions in SMA patients.
    Kesari A, Misra UK, Kalita J, Mishra VN, Pradhan S, Patil SJ, Phadke SR, Mittal B.
    J Neurol; 2005 Jun 03; 252(6):667-71. PubMed ID: 15772743
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  • 18. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals.
    Hahnen E, Forkert R, Marke C, Rudnik-Schöneborn S, Schönling J, Zerres K, Wirth B.
    Hum Mol Genet; 1995 Oct 03; 4(10):1927-33. PubMed ID: 8595417
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  • 19. 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 03; 84(8):465-9. PubMed ID: 17175684
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  • 20. SMA type 2 unrelated to chromosome 5q13.
    Nevo Y, Kramer U, Legum C, Shomrat R, Fatal A, Soffer D, Harel S, Shapira Y.
    Am J Med Genet; 1998 Jan 13; 75(2):193-5. PubMed ID: 9450884
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