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PUBMED FOR HANDHELDS

Journal Abstract Search

345 related items for PubMed ID: 16353285

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  • 23. [First case of successful pregnancy after preimplantation genetic diagnosis].
    Papp Z, Fancsovits P, Bán Z, Tóthné GZ, Urbancsek J.
    Orv Hetil; 2002 Dec 29; 143(52):2881-3. PubMed ID: 12638315
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  • 27. Duplex, triplex and quadruplex PCR for the preimplantation genetic diagnosis (PGD) of cystic fibrosis (CF), an exhaustive approach.
    Moutou C, Gardes N, Viville S.
    Prenat Diagn; 2004 Jul 29; 24(7):562-9. PubMed ID: 15300750
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  • 28. Gene changes in Duchenne muscular dystrophy: comparison of multiplex PCR and multiplex ligation-dependent probe amplification techniques.
    Kohli S, Saxena R, Thomas E, Singh J, Verma IC.
    Neurol India; 2010 Jul 29; 58(6):852-6. PubMed ID: 21150048
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  • 29. Preimplantation genetic diagnosis of Canavan disease.
    Yaron Y, Schwartz T, Mey-Raz N, Amit A, Lessing JB, Malcov M.
    Fetal Diagn Ther; 2005 Jul 29; 20(5):465-8. PubMed ID: 16113575
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  • 30. Preimplantation genetic diagnosis of skin fragility-ectodermal dysplasia syndrome.
    Fassihi H, Grace J, Lashwood A, Whittock NV, Braude PR, Pickering SJ, McGrath JA.
    Br J Dermatol; 2006 Mar 29; 154(3):546-50. PubMed ID: 16445790
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  • 31. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
    Pikó H, Vancsó V, Nagy B, Bán Z, Herczegfalvi A, Karcagi V.
    Neuromuscul Disord; 2009 Feb 29; 19(2):108-12. PubMed ID: 19084397
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  • 32. Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2.
    Kakourou G, Dhanjal S, Daphnis D, Doshi A, Nuttall S, Gotts S, Serhal P, Delhanty J, Harper J, SenGupta S.
    Prenat Diagn; 2007 Feb 29; 27(2):111-6. PubMed ID: 17192963
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  • 33. Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy.
    Huang WY, Hung CC, Lee CN, Su YN, Chen CP.
    Prenat Diagn; 2007 Jul 29; 27(7):653-6. PubMed ID: 17385798
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  • 36. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
    Ligon AH, Kashork CD, Richards CS, Shaffer LG.
    Eur J Hum Genet; 2000 Apr 29; 8(4):293-8. PubMed ID: 10854113
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  • 37. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 29; 56(3):105-52. PubMed ID: 19728970
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  • 40. Birth of healthy children after preimplantation diagnosis of beta-thalassemia.
    Jiao ZX, Zhuang GL, Zhou CQ, Shu YM, Li J, Liang XY.
    Chin Med J (Engl); 2004 Apr 29; 117(4):483-7. PubMed ID: 15109434
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