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Journal Abstract Search

144 related items for PubMed ID: 10589057

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  • 2. Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis.
    Moutou C, Gardes N, Viville S.
    Eur J Hum Genet; 2002 Apr; 10(4):231-8. PubMed ID: 12032730
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  • 5. Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (delta F508).
    Ao A, Ray P, Harper J, Lesko J, Paraschos T, Atkinson G, Soussis I, Taylor D, Handyside A, Hughes M, Winston RM.
    Prenat Diagn; 1996 Feb; 16(2):137-42. PubMed ID: 8650124
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  • 6. A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis.
    Thornhill AR, McGrath JA, Eady RA, Braude PR, Handyside AH.
    Prenat Diagn; 2001 Jun; 21(6):490-7. PubMed ID: 11438956
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  • 7. [First attempts in preimplantation genetic diagnosis: genetic analysis].
    Bán Z, Fancsovits P, Nagy B, Kamaszné HM, Urbancsek J, Papp Z.
    Orv Hetil; 2001 Nov 11; 142(45):2487-92. PubMed ID: 11778356
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  • 8. An efficient and reliable DNA extraction method for preimplantation genetic diagnosis: a comparison of allele drop out and amplification rates using different single cell lysis methods.
    Kim SA, Yoon JA, Kang MJ, Choi YM, Chae SJ, Moon SY.
    Fertil Steril; 2009 Aug 11; 92(2):814-8. PubMed ID: 18706553
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  • 11. Multiplex allele-specific target amplification based on PCR suppression.
    Broude NE, Zhang L, Woodward K, Englert D, Cantor CR.
    Proc Natl Acad Sci U S A; 2001 Jan 02; 98(1):206-11. PubMed ID: 11136256
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  • 13. [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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  • 14. [Preclinical study of preimplantation genetic diagnosis in animal].
    Ji Y, Zhao Y, Sheng Y.
    Zhonghua Fu Chan Ke Za Zhi; 2000 Aug 29; 35(8):462-4. PubMed ID: 11776197
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  • 15. Allele-specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy.
    Moutou C, Gardes N, Rongières C, Ohl J, Bettahar-Lebugle K, Wittemer C, Gerlinger P, Viville S.
    Prenat Diagn; 2001 Jun 29; 21(6):498-503. PubMed ID: 11438957
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  • 17. A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosis.
    Vrettou C, Palmer G, Kanavakis E, Tzetis M, Antoniadi T, Mastrominas M, Traeger-Synodinos J.
    Prenat Diagn; 1999 Dec 29; 19(13):1209-16. PubMed ID: 10660957
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