Fluorescence in situ hybridization in the study of chromosomal abnormalities;Fluorescentie-in-situhybridisatie bij het onderzoek naar chromosomale afwijkingen

Nederlands Tijdschrift voor Geneeskunde

Volumn 143, Issue 45, 1999, Pages 2265-2268

  Hoovers, J M N ^a   Mellink, C H M ^a   Leschot, N J ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AMNION FLUID CYTOLOGY; AMNIOTIC FLUID CELL; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CYTOGENETICS; DIGEORGE SYNDROME; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; SEQUENCE ANALYSIS; TRISOMY; WILLIAMS BEUREN SYNDROME;

CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CYTOGENETIC ANALYSIS; DNA MUTATIONAL ANALYSIS; DNA PROBES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICROSATELLITE REPEATS; SYNDROME; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0033530385     PISSN: 00282162     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

1. Tanke HJ, Wiegant J, Gijlswijk RPM van, Bezrookove V, Pattenier H, Heetebrij RJ, et al. New strategy for multi-colour fluorescence in situ hybridisation: COBRA: combined binary ratio labelling. Eur J Hum Genet 1999;7:2-11.
2. Flint J, Wilkie AOM, Buckle VJ, Winter RM, Holland AJ, McDermid HE. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat Genet 1995;9: 132-40.
3. Bijlsma EK, Aalfs CM, Sluijter S, Oude Luttikhuis MEM, Trembath RC, Hoovers JMN, et al. Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype. J Med Genet 1999;36: 604-9.
4. Eiben B, Trawicki W, Hammans W, Goebel R, Epplen JT. A prospective comparative study on fluorescence in situ hybridization (FISH) of uncultured amniocytes and standard karyotype analysis. Prenat Diagn 1998;18:901-6.
5. Opstal D van. Molecular cytogenetics in prenatal diagnosis [proefschrift]. Rotterdam: Erasmus Universiteit; 1998.
6. Jalal SM, Law ME. Detection of newborn aneuploidy by interphase fluorescence in situ hybridization. Mayo Clin Proc 1997;72:705-10.
7. Graaf IM de, Bezouw SMCA van, Jakobs ME, Leschot NJ, Zondervan HA, Bilardo CM, et al. First-trimester non-invasive prenatal diagnosis of triploidy. Prenat Diagn 1999;19:175-7.
8. Graaf IM de, Jakobs ME, Leschot NJ, Ravkin I, Goldbard S, Hoovers JMN. Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system. Prenat Diagn 1999;19:648-52.
9. Dauwerse HG, Smit EME, Giles RH, Slater R, Breuning MH, Hagemeijer A, et al. Two-color FISH detection of the inv(16) in interphase nuclei of patients with acute myeloid leukemia. Br J Haematol 1999;106:111-4.
10. Marshall A, Hodgson J. DNA chips: an array of possibilities. Nat Biotechnol 1998:16:27-31.
11. Pinkel D, Segraves R, Sudar D, Clark S, Poole I, Kowbel D, et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 1998;20: 207-11.
12. Pollack JR, Perou CM, Alizadeh AA, Eisen MB, Pergamenschikov A, Williams CF, et al. Genome-wide analysis of DNA copy-number changes using cDNA microarrays. Nat Genet 1999;23:41-6.
13. Karnebeek CDM van, Hennekam RCM. Associations between chromosomal anomalies and congenital heart defects: a database search. Am J Med Genet 1999;84:158-66.