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Journal Abstract Search
926 related items for PubMed ID: 15583993
21. [Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells]. Marguerat P, Gaide AC, Thonney F, Schorderet D. Rev Med Suisse Romande; 2000 May; 120(5):401-7. PubMed ID: 10911743 [Abstract] [Full Text] [Related]
22. Prenatal diagnosis by rapid aneuploidy detection and karyotyping: a prospective study of the role of ultrasound in 1589 second-trimester amniocenteses. Leung WC, Waters JJ, Chitty L. Prenat Diagn; 2004 Oct; 24(10):790-5. PubMed ID: 15503279 [Abstract] [Full Text] [Related]
23. [Application of multicolor primed in situ labeling in simultaneous identification of chromosomes 18, X and Y in uncultured amniocytes]. Deng L, Ding XP, Nie Y, Hu Y, Ren HJ. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):439-42. PubMed ID: 20017312 [Abstract] [Full Text] [Related]
24. [Rapid prenatal diagnosis of Down's syndrome in the first trimester of pregnancy by fluorescence in situ hybridization]. Xiang Y, Sun N, Wang F. Zhonghua Fu Chan Ke Za Zhi; 1997 Nov; 32(11):646-8. PubMed ID: 9639761 [Abstract] [Full Text] [Related]
25. Interphase fluorescence in situ hybridization in a Turner syndrome variant with IsoXq. A case report. Chang SD, Lin SL, Chen FP, Chu KK. J Reprod Med; 1996 Mar; 41(3):175-8. PubMed ID: 8778416 [Abstract] [Full Text] [Related]
26. False-positive diagnosis of trisomy 21 using fluorescence in situ hybridisation (FISH) on uncultured amniotic fluid cells. George AM, Oei P, Winship I. Prenat Diagn; 2003 Apr; 23(4):302-5. PubMed ID: 12673634 [Abstract] [Full Text] [Related]
27. Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, and X by quantitative fluorescence polymerase chain reaction. Ochshorn Y, Bar-Shira A, Jonish A, Yaron Y. Fetal Diagn Ther; 2006 Apr; 21(4):326-31. PubMed ID: 16757905 [Abstract] [Full Text] [Related]
28. [Interphase FISH test as a rapid test for trisomies in amniotic fluid--results of a prospective study]. Bink K, Pauer HU, Bartels I. Z Geburtshilfe Neonatol; 2000 Apr; 204(1):8-13. PubMed ID: 10721180 [Abstract] [Full Text] [Related]
29. Prenatal detection of isochromosome 21 by QF-PCR. A comparison between FISH and traditional karyotyping. Gole L, Lian NB, Lian NP, Rauff M, Biswas A, Choolani M. Fetal Diagn Ther; 2008 Apr; 24(1):47-50. PubMed ID: 18504381 [Abstract] [Full Text] [Related]
30. FastFISH: technique for ultrarapid fluorescence in situ hybridization on uncultured amniocytes yielding results within 2 h of amniocentesis. Choolani M, Ho SS, Razvi K, Ponnusamy S, Baig S, Fisk NM, Biswas A, Rapid Molecular Testing in Prenatal Diagnosis Group. Mol Hum Reprod; 2007 Jun; 13(6):355-9. PubMed ID: 17430982 [Abstract] [Full Text] [Related]
31. Application of multi-PRINS to simultaneously identify chromosomes 18, X, and Y in prenatal diagnosis. Gadji M, Krabchi K, Yan J, Drouin R. Methods Mol Biol; 2008 Jun; 444():49-58. PubMed ID: 18425471 [Abstract] [Full Text] [Related]
32. [Identification of aneuploids in uncultured amniotic fluid cells by interphase fluorescence in situ hybridization]. Sohda M, Harada N, Nishimura T, Noda K, Abe K, Niikawa N. Rinsho Byori; 1998 May; 46(5):486-92. PubMed ID: 9627501 [Abstract] [Full Text] [Related]
33. Role of amniotic fluid interphase fluorescence in situ hybridization (FISH) analysis in patient management. Cheong Leung W, Chitayat D, Seaward G, Windrim R, Ryan G, Barrett J, Winsor EJ. Prenat Diagn; 2001 Apr; 21(4):327-32. PubMed ID: 11288128 [Abstract] [Full Text] [Related]
34. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment. Caine A, Maltby AE, Parkin CA, Waters JJ, Crolla JA, UK Association of Clinical Cytogeneticists (ACC). Lancet; 2001 Apr; 366(9480):123-8. PubMed ID: 16005334 [Abstract] [Full Text] [Related]
35. [Analysis of 89 amniotic samples using fluorescent in situ hybridization]. Wei P, Li YX, Zeng L, Chen C, Qin SF, Wang XY, Xi N, Tang SQ, Leng M, Liu CL. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):214-7. PubMed ID: 23568739 [Abstract] [Full Text] [Related]
36. FlashFISH: "same day" prenatal diagnosis of common chromosomal aneuploidies. Ho SS, Choolani MA. Methods Mol Biol; 2010 Apr; 659():261-8. PubMed ID: 20809318 [Abstract] [Full Text] [Related]
37. Amniotic fluid interphase fluorescence in situ hybridization (FISH) for detection of aneuploidy; experiences in 130 prenatal cases. Lim HJ, Kim YJ, Yang JH, Kim EJ, Choi JS, Jung SH, Ahn HK, Han JY, Kim MY, Choi KH, Kim JM, Kim YM, Park SY, Ryu HM. J Korean Med Sci; 2002 Oct; 17(5):589-92. PubMed ID: 12378006 [Abstract] [Full Text] [Related]
40. Down syndrome with pure partial trisomy 21q22 due to a paternal insertion (4;21) uncovered by uncultured amniotic fluid interphase FISH. Lee J, Stanley JR, Vaz SA, Mulvihill JJ, Wilson P, Hopcus-Niccum D, Li S. Am J Med Genet A; 2005 Jan 15; 132A(2):206-8. PubMed ID: 15578618 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]