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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

396 related items for PubMed ID: 15910686

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  • 3. Population screening and cascade testing for carriers of SMA.
    Smith M, Calabro V, Chong B, Gardiner N, Cowie S, du Sart D.
    Eur J Hum Genet; 2007 Jul; 15(7):759-66. PubMed ID: 17392705
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  • 7. Genetic testing and risk assessment for spinal muscular atrophy (SMA).
    Ogino S, Wilson RB.
    Hum Genet; 2002 Dec; 111(6):477-500. PubMed ID: 12436240
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  • 10. Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophy.
    Arkblad EL, Darin N, Berg K, Kimber E, Brandberg G, Lindberg C, Holmberg E, Tulinius M, Nordling M.
    Neuromuscul Disord; 2006 Dec; 16(12):830-8. PubMed ID: 17049859
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  • 11. Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system.
    Shaw SW, Cheng PJ, Chang SD, Lin YT, Hung CC, Chen CP, Su YN.
    Acta Obstet Gynecol Scand; 2008 Dec; 87(9):960-8. PubMed ID: 18720039
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  • 14. Genetic risk assessment in carrier testing for spinal muscular atrophy.
    Ogino S, Leonard DG, Rennert H, Ewens WJ, Wilson RB.
    Am J Med Genet; 2002 Jul 15; 110(4):301-7. PubMed ID: 12116201
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  • 18. [Quantitative analysis of the genes determining spinal muscular atrophy].
    Nagymihály M, Herczegfalvi A, Tímár L, Karcagi V.
    Ideggyogy Sz; 2009 Nov 30; 62(11-12):390-7. PubMed ID: 20025129
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  • 19. Spinal muscular atrophy diagnostics.
    Prior TW.
    J Child Neurol; 2007 Aug 30; 22(8):952-6. PubMed ID: 17761649
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