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Journal Abstract Search


262 related items for PubMed ID: 12875676

  • 1. Prenatal diagnosis of Werdnig-Hoffmann disease in China.
    Feng J, Toshiyuki Y.
    Chin Med J (Engl); 2003 May; 116(5):673-5. PubMed ID: 12875676
    [Abstract] [Full Text] [Related]

  • 2. Prenatal prediction of spinal muscular atrophy by SMN deletion analysis.
    Dhamcharee V, Mutirangura A, Tannirandom Y, Jongpiputvanich S, Romyanan O.
    Southeast Asian J Trop Med Public Health; 1999 May; 30 Suppl 2():186-7. PubMed ID: 11400766
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  • 3. 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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  • 4. Prenatal diagnosis of spinal muscular atrophy type I (Werdnig- hoffmann) by DNA deletion analysis of cultivated amniocytes.
    Stipoljev F, Sertić J, Latin V, Rukavina-Stavljenić A, Kurjak A.
    Croat Med J; 1999 Sep 05; 40(3):433-7. PubMed ID: 10411975
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  • 5. [Gene diagnosis for spinal muscular atrophy and its application study].
    Cao DH, Ren MH, Lin CK, Cui WT, Ma HW, Wu YY, Jin CL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 05; 26(3):306-9. PubMed ID: 19504445
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  • 6. Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families.
    Savas S, Eraslan S, Kantarci S, Karaman B, Acarsoz D, Tükel T, Cogulu O, Ozkinay F, Basaran S, Aydinli K, Yuksel-Apak M, Kirdar B.
    Prenat Diagn; 2002 Aug 05; 22(8):703-9. PubMed ID: 12210580
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  • 9. 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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  • 10. 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 05; 64(2):225-31. PubMed ID: 17296838
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  • 11. Preserved umbilical cord facilitates antenatal diagnosis of spinal muscular atrophy.
    Kabra M, Arora S, Maria A, Aggarwal R.
    Indian Pediatr; 2003 May 05; 40(5):415-8. PubMed ID: 12768044
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  • 12. [Werdnig-Hoffmann disease. The first prenatal diagnosis in Cuba].
    Acevedo-López AM, Zaldívar-Vaillant T, Hernández-Chico C, Moreno F, Rosich-Capablanca G, Guerra-Badía R.
    Rev Neurol; 2003 May 05; 29(12):1172-5. PubMed ID: 10652743
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  • 13. Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs).
    Essawi ML, Al-Attribi GM, Gaber KR, El-Harouni AA.
    Gene; 2012 Nov 01; 509(1):120-3. PubMed ID: 22921322
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  • 16. [Survival motor neuron gene and neuronal apoptosis inhibitory protein gene deletion in patients with spinal muscular atrophy].
    Ma S, Yuan L, Liu T, Yang T, Zhou W, Wu H.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2000 Dec 01; 22(6):551-4. PubMed ID: 12903402
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  • 17. Genetic diagnosis of Werdnig-Hoffmann disease: a problem for application to prenatal diagnosis.
    Migita M, Migita M, Uchikoba Y, Orimo H, Shimada T, Shimada T, Matsumoto T, Hayakawa J, Fujino O, Saitoh M, Fukunaga Y.
    J Nippon Med Sch; 2003 Feb 01; 70(1):45-8. PubMed ID: 12646976
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  • 18. [An analysis of chimeric SMN genes--new possibilities in the study of the molecular genetic nature of mutations and in the diagnosis of spinal muscular atrophy (SMA)].
    Ekshiian AIu, Livshits LA.
    Tsitol Genet; 1999 Feb 01; 33(3):21-6. PubMed ID: 10474859
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  • 19. [A molecular genetic analysis of spinal muscular atrophy (SMA) in families at high risk from different regions of Ukraine].
    Ekshiian AIu, Livshits LA, Bychkova AM, Afanas'eva NA, Bariliak IR.
    Tsitol Genet; 1997 Feb 01; 31(6):75-81. PubMed ID: 9591348
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  • 20. 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
    [Abstract] [Full Text] [Related]


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