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Journal Abstract Search

343 related items for PubMed ID: 19365952

  • 21. Prenatal diagnosis of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 intragenomic deoxyribonucleic acid probes.
    Katayama S, Yano T, Takeshita N, Abe Y, Usui A, Kubo H, Momose K, Ubagai T.
    Nihon Sanka Fujinka Gakkai Zasshi; 1991 Jun; 43(6):633-40. PubMed ID: 1677375
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  • 22. First trimester chorionic villus sampling for DNA analysis.
    Bolodár A, Horváth K, Németi M, Papp Z.
    Acta Univ Carol Med (Praha); 1990 Jun; 36(1-4):129-31. PubMed ID: 2130673
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  • 23. Transabdominal chorionic villus sampling: experience at Maharaj Nakorn Chiang Mai Hospital.
    Sirichotiyakul S, Piyamongkol W, Tongprasert F, Srisupandit K, Luewan S.
    J Med Assoc Thai; 2008 Jun; 91(6):813-7. PubMed ID: 18697378
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  • 26. Early second trimester (13 to 20 weeks) transabdominal chorionic villus sampling (TA-CVS): a safe and alternative method for both high and low risk populations.
    Brambati B, Tului L, Camurri L, Guercilena S.
    Prenat Diagn; 2002 Oct; 22(10):907-13. PubMed ID: 12378575
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  • 27. 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; 27(7):653-6. PubMed ID: 17385798
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  • 28. Detection of cell-free fetal DNA in maternal urine.
    Illanes S, Denbow ML, Smith RP, Overton TG, Soothill PW, Finning K.
    Prenat Diagn; 2006 Dec; 26(13):1216-8. PubMed ID: 17139694
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  • 31. Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism.
    Camire R, Ann Denchy R, Day GA, Lanzano P, Sheth S, Brown S.
    Prenat Diagn; 2003 Jun; 23(6):457-60. PubMed ID: 12813758
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  • 32. Randomized study of early amniocentesis versus chorionic villus sampling: a technical and cytogenetic comparison of 650 patients.
    Byrne D, Marks K, Azar G, Nicolaides K.
    Ultrasound Obstet Gynecol; 1991 Jul 01; 1(4):235-40. PubMed ID: 12797050
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  • 39. Screening for DMD/BMD deletion carriers by fluorescence in situ hybridization.
    Xiao Y, Jiang X, Wang R.
    Genet Test; 2003 Jul 01; 7(3):195-201. PubMed ID: 14641995
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  • 40. Prenatal diagnosis of the carbohydrate-deficient glycoprotein syndrome type 1A (CDG1A) by a combination of enzymology and genetic linkage analysis after amniocentesis or chorionic villus sampling.
    Charlwood J, Clayton P, Keir G, Mian N, Young E, Winchester B.
    Prenat Diagn; 1998 Jul 01; 18(7):693-9. PubMed ID: 9706650
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