The application of fluorescence in-situ hybridization to prenatal diagnosis

Current Opinion in Obstetrics and Gynecology

Volumn 12, Issue 2, 2000, Pages 73-76

  Pergament, E ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; ARTICLE; CHROMOSOME ABERRATION; COMPARATIVE GENOMIC HYBRIDIZATION; DNA PROBE; FETUS CELL; FETUS DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC DISORDER; HUMAN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TELOMERE;

CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PREGNANCY; PREIMPLANTATION DIAGNOSIS; PRENATAL DIAGNOSIS;

EID: 0034465731     PISSN: 1040872X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001703-200004000-00003     Document Type: Article

References (33)

1. Prenatal interphase fluorescence in situ hybridization (FISH) policy statement
2. Rapid prenatal diagnosis of ameuploidies in uncultured amniocytes by fluorescence in situ hybridization
3. The clinical application of interphase FISH in prenatal diagnosis
4. Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies
5. Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation
6. Prenatal detection of extra structurally abnormal chromosomes (ESACs): New cases and a review of the literature
7. Prenatal evaluation of a de novo X;9 translocation
8. Unexpected inherited chromosomal translocation during prenatal diagnosis for maternal age: Risk for a nondetectable karyotype imbalance in offspring
9. Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH)
10. Molecular, cytogenetic and clinical characterization of six XX males including one prenatal diagnosis
11. Pallister-Killian syndrome [I(12)]: First pre-natal diagnosis using cordocentesis in the second trimester confirmed by in situ hybridization
12. Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescence in situ hybridization
13. Prenatal diagnosis by FISH in a family with Pelizaeus-Merzbacher disease caused by duplication of PLP gene
14. Detection of fetal cells with common chromosomal aneuploidies in maternal blood
15. Investigation of maternal blood enriched for fetal cells: Role in screening and diagnosis of fetal trisomies
16. Prenatal diagnosis on fetal cells obtained from maternal blood: Report of 66 cases
17. Enrichment, identification and analysis of fetal cells from maternal blood: Evaluation of a prenatal diagnosis system
18. Improvement of fetal cell recovery from maternal blood: Suitable density gradient for FACS separation
19. Differential development of fetal and adult haemoglobin profiles in colony culture: Isolation of fetal nucleated red cells by two-colour fluorescence labelling
20. Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: Identification of the categories for which it should be proposed
21. Preimplantation genetic diagnosis for couples at high risk of Down syndrome prenancy owing to parental translocation or mosaicism
22. Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22)
23. Chromosome translocations: Segregation modes and strategies for preimplantation genetic diagnosis
24. Case report: Chromatid exchange and predivision of chromatids as other sources of abnormal oocytes detected by preimplantation genetic diagnosis of translocations
25. Preimplantation genetic diagnosis of aneuploid: Were we looking at the wrong chromosomes?
26. Increased chromosome abnormalities in human preimplantation embryos after in-vitro fertilization in patients with recurrent miscarriage
27. Identification of de novo chromosomal markers and derivatives by spectal karyotyping
28. Multiplex-FISH for pre- and postnatal diagnostic applications
29. Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics
30. High resolution multicolor-banding: A new technique for reined FISH analysis of human chromosomes
31. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16
32. Detection of numerical chromosome aberrations by comparative genome hybridization
33. Screening of human placentas for chromosomal mosaicism using comparative genomic hybridization