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Journal Abstract Search

351 related items for PubMed ID: 12032730

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  • 4. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.
    Casals T, Gimenez J, Ramos MD, Nunes V, Estivill X.
    Prenat Diagn; 1996 Mar; 16(3):215-22. PubMed ID: 8710774
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  • 8. Single intragenic microsatellite preimplantation genetic diagnosis for cystic fibrosis provides positive allele identification of all CFTR genotypes for informative couples.
    Eftedal I, Schwartz M, Bendtsen H, Andersen AN, Ziebe S.
    Mol Hum Reprod; 2001 Mar; 7(3):307-12. PubMed ID: 11228252
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  • 9. [Successful preimplantation genetic diagnosis for beta-thalassemia using multiplex nested polymerase chain reaction].
    Deng J, Zhuang GL, Peng WL, Zhou CQ, Li J, Liang XY, Deng MF, Zeng YH, Sun HY.
    Zhonghua Yi Xue Za Zhi; 2005 Mar 30; 85(12):811-5. PubMed ID: 15949396
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  • 10. Preimplantation genetic diagnosis for cystic fibrosis: the Montpellier center's 10-year experience.
    Girardet A, Ishmukhametova A, Willems M, Coubes C, Hamamah S, Anahory T, Des Georges M, Claustres M.
    Clin Genet; 2015 Feb 30; 87(2):124-32. PubMed ID: 24762087
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  • 11. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.
    J Cyst Fibros; 2008 Mar 30; 7(2):102-9. PubMed ID: 17662673
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  • 12. PGD for autosomal dominant polycystic kidney disease type 1.
    De Rycke M, Georgiou I, Sermon K, Lissens W, Henderix P, Joris H, Platteau P, Van Steirteghem A, Liebaers I.
    Mol Hum Reprod; 2005 Jan 30; 11(1):65-71. PubMed ID: 15591452
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  • 13. PGD on a recombinant allele: crossover between the TSC2 gene and 'linked' markers impairs accurate diagnosis.
    Altarescu G, Eldar Geva T, Brooks B, Margalioth E, Levy-Lahad E, Renbaum P.
    Prenat Diagn; 2008 Oct 30; 28(10):929-33. PubMed ID: 18792920
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  • 18. Improving clinical preimplantation genetic diagnosis for cystic fibrosis by duplex PCR using two polymorphic markers or one polymorphic marker in combination with the detection of the DeltaF508 mutation.
    Goossens V, Sermon K, Lissens W, De Rycke M, Saerens B, De Vos A, Henderix P, Van de Velde H, Platteau P, Van Steirteghem A, Devroey P, Liebaers I.
    Mol Hum Reprod; 2003 Sep 30; 9(9):559-67. PubMed ID: 12900515
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  • 19. Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation delta F508 by fluorescent polymerase chain reaction.
    Moutou C, Viville S.
    Prenat Diagn; 1999 Dec 30; 19(13):1248-50. PubMed ID: 10660962
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