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Journal Abstract Search

181 related items for PubMed ID: 10980532

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  • 10. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA).
    Wirth B.
    Hum Mutat; 2000; 15(3):228-37. PubMed ID: 10679938
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  • 12. Implementation of SMA carrier testing in genetic laboratories: comparison of two methods for quantifying the SMN1 gene.
    Cuscó I, Barceló MJ, Baiget M, Tizzano EF.
    Hum Mutat; 2002 Dec; 20(6):452-9. PubMed ID: 12442269
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  • 13. Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests.
    Botta A, Tacconelli A, Bagni I, Giardina E, Bonifazi E, Pietropolli A, Clementi M, Novelli G.
    Neurology; 2005 Nov 22; 65(10):1631-5. PubMed ID: 16301493
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  • 16. [Quantitative analysis of SMN gene copies in spinal muscular atrophy].
    Ding HX, Yang XS, Xiao B, Wu ZG, Zhang LF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr 22; 21(2):153-5. PubMed ID: 15079799
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  • 17. Quantification of SMN1 and SMN2 genes by capillary electrophoresis for diagnosis of spinal muscular atrophy.
    Wang CC, Chang JG, Ferrance J, Chen HY, You CY, Chang YF, Jong YJ, Wu SM, Yeh CH.
    Electrophoresis; 2008 Jul 22; 29(13):2904-11. PubMed ID: 18546169
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  • 20. Quantification of PCR bias caused by a single nucleotide polymorphism in SMN gene dosage analysis.
    Ogino S, Wilson RB.
    J Mol Diagn; 2002 Nov 22; 4(4):185-90. PubMed ID: 12411585
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