Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2‐year multi‐center retrospective study and review of the literature
暂无分享,去创建一个
P. N. Rao | M. Schoonmaker | H. Wyandt | M. Pettenati | J. Tepperberg | J Tepperberg | M J Pettenati | P N Rao | C M Lese | D Rita | H Wyandt | S Gersen | B White | M M Schoonmaker | D. Rita | S. Gersen | C. Lese | P. Rao | B. White | Christa M. Lese
[1] H. Willard,et al. Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome. , 1985, Journal of molecular biology.
[2] E. Beinder,et al. Aneuploidiediagnostik mittels Fluoreszenz-in-situ-Hybridisierung (FISH); Stellenwert bei Schwangerschaften mit erhöhtem Risiko für Chromosomenaberrationen , 2000 .
[3] R. Pike. Technical and clinical assessment of fluorescence in situ hybridization: An ACMG/ASHG position statement. I. Technical considerations: Test and Technology Transfer Committee , 2000, Genetics in Medicine.
[4] J. Philip,et al. PRENATAL DETECTION OF CHROMOSOME ANEUPLOIDIES BY FLUORESCENCE IN SITU HYBRIDIZATION: EXPERIENCE WITH 2000 UNCULTURED AMNIOTIC FLUID SAMPLES IN A PROSPECTIVE PRECLINICAL TRIAL , 1997 .
[5] B. Thilaganathan,et al. Effectiveness of prenatal chromosomal analysis using multicolour fluorescent in situ hybridisation , 2000, BJOG : an international journal of obstetrics and gynaecology.
[6] L. Taine,et al. False‐negative results of trisomy 21 on direct analysis on chorionic villus sampling , 1998, Prenatal diagnosis.
[7] J. Epplen,et al. False‐negative finding in rapid interphase FISH analysis of uncultured amniotic cells , 1999, Prenatal diagnosis.
[8] J. Gray,et al. A degenerate alpha satellite probe, detecting a centromeric deletion on chromosome 21 in an apparently normal human male, shows limitations of the use of satellite DNA probes for interphase ploidy analysis. , 1992, Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology.
[9] W. Holzgreve,et al. Fluorescent in situ hybridization utilization for high-risk prenatal diagnosis: a trade-off among speed, expense, and inherent limitations of chromosome-specific probes. , 1994, American journal of obstetrics and gynecology.
[10] A. B. Reese. Tumors of the eye , 1976 .
[11] J W Gray,et al. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[12] E. Pergament,et al. The clinical application of interphase FISH in prenatal diagnosis , 2000, Prenatal diagnosis.
[13] G. Dewald,et al. Prenatal detection of aneuploidy by directly labeled multicolored probes and interphase fluorescence in situ hybridization. , 1998, Mayo Clinic proceedings.
[14] T. N. Abdella,et al. Genetic amniocentesis: a twelve years' experience. , 1985, American journal of medical genetics.
[15] K. Kennedy,et al. The need to reevaluate trisomy screening for advanced maternal age in prenatal diagnosis. , 1993, American journal of obstetrics and gynecology.
[16] K. Klinger,et al. Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells. , 1992, Human molecular genetics.
[17] E. Pergament,et al. Hybridization of chromosome 18 alpha‐satellite DNA probe to chromosome 22 , 1998, Prenatal diagnosis.
[18] G. Robinson,et al. Impact of prenatal testing on maternal-fetal bonding: chorionic villus sampling versus amniocentesis. , 1991, American journal of obstetrics and gynecology.
[19] P. Lewin,et al. Defining the efficiency of fluorescence in situ hybridization on uncultured amniocytes on a retrospective cohort of 27407 prenatal diagnoses , 2000, Prenatal diagnosis.
[20] J. Oury,et al. Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization , 1994, Prenatal diagnosis.
[21] J. R. Beekhuis,et al. The predictive value of cytogenetic diagnosis after CVS: 1500 cases , 1990, Prenatal diagnosis.
[22] K. Klinger,et al. Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens. , 1993, American journal of human genetics.
[23] K. Klinger,et al. Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH). , 1992, American journal of human genetics.
[24] C. Epstein,et al. Prenatal genetic diagnosis in 3000 amniocenteses. , 1979, The New England journal of medicine.
[25] S. R. Young,et al. Low fluorescence alpha satellite region yields negative result , 1992, Prenatal diagnosis.
[26] C. Strom,et al. Cross‐hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by fish , 1995, Prenatal diagnosis.
[27] R. Lebo,et al. Rapid aneuploid diagnosis of high-risk fetuses by fluorescence in situ hybridization. , 1996, American journal of obstetrics and gynecology.
[28] G. Barkai,et al. Use of interphase fluorescence in situ hybridization in third trimester fetuses with anomalies and growth retardation. , 1999, American journal of medical genetics.
[29] A. Tóth,et al. Cross-hybridization of the chromosome 13/21 alpha satellite DNA to chromosome 22 or a rare polymorphism? , 1997, Prenatal diagnosis.
[30] K. Nicolaides,et al. International, collaborative assessment of 146,000 prenatal karyotypes: expected limitations if only chromosome-specific probes and fluorescent in-situ hybridization are used. , 1999, Human reproduction.
[31] N. Uddenberg,et al. Prenatal diagnosis for psychological reasons: Comparison with other indications, advanced maternal age and known genetic risk , 1990, Prenatal diagnosis.
[32] K. Bink,et al. [Interphase FISH test as a rapid test for trisomies in amniotic fluid--results of a prospective study]. , 2000, Zeitschrift für Geburtshilfe und Neonatologie.
[33] F. Malone,et al. Defining the role of fluorescence in situ hybridization on uncultured amniocytes for prenatal diagnosis of aneuploidies. , 1997, American journal of obstetrics and gynecology.
[34] S. Mercier,et al. Prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization on uncultured amniotic cells: experience with 630 samples. , 1995, Annales de genetique.
[35] B. Eiben,et al. Rapid Prenatal Diagnosis of Aneuploidies in Uncultured Amniocytes by Fluorescence in situ Hybridization , 1999, Fetal Diagnosis and Therapy.
[36] Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies , 1999, Prenatal diagnosis.
[37] S. Michie,et al. The psychological effects of false‐positive results in prenatal screening for fetal abnormality: A prospective study , 1992, Prenatal diagnosis.
[38] A. N. Lamb,et al. Overwhelming maternal cell contamination in amniotic fluid samples from patients with oligohydramnios can lead to false prenatal interphase FISH results , 1999, Prenatal diagnosis.
[39] B. Ward,et al. MATERNAL CELL CONTAMINATION IN UNCULTURED AMNIOTIC FLUID , 1996, Prenatal diagnosis.
[40] M. Evans,et al. Routine prenatal diagnosis of aneuploidy by FISH studies in high-risk pregnancies. , 2000, American journal of medical genetics.
[41] K. Klinger,et al. Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH. , 1996, American journal of human genetics.
[42] Y. Lam,et al. Clinical significance of amniotic‐fluid‐cell culture failure , 1998, Prenatal Diagnosis.
[43] J. Wauters,et al. Incidence of low-fluorescence alpha satellite region on chromosome 21 escaping detection of aneuploidy at interphase by FISH. , 1995, Cytogenetics and Cell Genetics.
[44] W. Sepulveda,et al. Amniotic fluid culture failure: clinical significance and association with aneuploidy , 1996, Obstetrics and gynecology.
[45] S. Dyack,et al. Risk of false‐positive prenatal diagnosis using interphase FISH testing: hybridization of alpha‐satellite X probe to chromosome 19 , 1999, Prenatal diagnosis.
[46] A. Seres-Santamaria,et al. Fluorescent in-situ hybridisation and Down's syndrome , 1993, The Lancet.
[47] D. Spathas,et al. Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study , 1994, Prenatal diagnosis.
[48] R. Verma,et al. Variations in alphoid DNA sequences escape detection of aneuploidy at interphase by FISH technique. , 1992, Genomics.
[49] D. Van Opstal,et al. False‐negative findings in chorionic villi , 1999, Prenatal Diagnosis.
[50] R. Glazier,et al. Psychological outcomes following maternal serum screening: a cohort study. , 1998, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.
[51] D. Ledbetter,et al. The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities. , 1989, The New England journal of medicine.
[52] P. Devilee,et al. Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21. , 1986, Cytogenetics and cell genetics.