Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities

Annales de Genetique

Volumn 41, Issue 3, 1998, Pages 133-140

  Lapierre, J M ^a   Cacheux, V ^a   Collot, N ^a   Da Silva, F ^a   Hervy, N ^a   Rivet, D ^a   Romana, S ^a   Wiss, J ^a   Benzaken, B ^a   Aurias, A ^a   Tachdjian, G ^a  

^a HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

CGH; Chromosomal abnormalities; Comparative genomic hybridization; Cytogenetics; Prenatal

Indexed keywords

REAGENT;

AMNION FLUID; ARTICLE; BLOOD CULTURE; CHORION VILLUS; CHROMOSOME 12P; CHROMOSOME 5P; CHROMOSOME 9P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION 10; CHROMOSOME TRANSLOCATION 5; CLINICAL ARTICLE; COMPUTER PROGRAM; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; DNA HYBRIDIZATION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; MALE; MICROSCOPE; MONOSOMY; MONOSOMY X; PRADER WILLI SYNDROME; PRENATAL DIAGNOSIS; TETRASOMY; TRISOMY 13; TRISOMY 18; TRISOMY 21; X CHROMOSOME ABERRATION;

AMNIOTIC FLUID; CHORIONIC VILLI; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; GENOME, HUMAN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; NUCLEIC ACID HYBRIDIZATION; PRENATAL DIAGNOSIS; SIGNAL PROCESSING, COMPUTER-ASSISTED;

EID: 0031791316     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)