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Journal Abstract Search

203 related items for PubMed ID: 16049987

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  • 2. Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.
    Chen WJ, Wu ZY, Lin MT, Su JF, Lin Y, Murong SX, Wang N.
    Arch Neurol; 2007 Feb; 64(2):225-31. PubMed ID: 17296838
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  • 3. 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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  • 11. Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene.
    Moutou C, Machev N, Gardes N, Viville S.
    Prenat Diagn; 2006 Nov 22; 26(11):1037-41. PubMed ID: 16941715
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  • 12. Prenatal diagnosis of spinal muscular atrophy in Chinese by genetic analysis of fetal cells.
    Wu T, Ding XS, Li WL, Yao J, Deng XX.
    Chin Med J (Engl); 2005 Aug 05; 118(15):1274-7. PubMed ID: 16117881
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  • 14. Spinal muscular atrophy genetic testing experience at an academic medical center.
    Ogino S, Leonard DG, Rennert H, Wilson RB.
    J Mol Diagn; 2002 Feb 05; 4(1):53-8. PubMed ID: 11826188
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  • 15. 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 05; 24(10):1052-4. PubMed ID: 14578966
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  • 16. Determination of SMN1 and SMN2 copy number using TaqMan technology.
    Anhuf D, Eggermann T, Rudnik-Schöneborn S, Zerres K.
    Hum Mutat; 2003 Jul 05; 22(1):74-8. PubMed ID: 12815596
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  • 17. 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 05; 20(6):452-9. PubMed ID: 12442269
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  • 18. Prenatal diagnosis for risk of spinal muscular atrophy.
    Cuscó I, Barceló MJ, Soler C, Parra J, Baiget M, Tizzano E.
    BJOG; 2002 Nov 05; 109(11):1244-9. PubMed ID: 12452462
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  • 19. [Genetic diagnosis and prenatal diagnosis of spinal muscular atrophy by restriction endonucleases digestion of PCR product].
    Li Q, Ma Y, Pan Q.
    Zhonghua Yi Xue Za Zhi; 2001 Dec 10; 81(23):1447-9. PubMed ID: 11930619
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