Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping

Prenatal Diagnosis

Volumn 19, Issue 12, 1999, Pages 1143-1149

  Peschka, Bärbel ^a   Leygraaf, J ^b   Hansmann, D ^b   Hansmann, M ^a   Schrock E ^c   Ried, T ^c   Engels, H ^a   Schwanitz, G ^a   Schubert, R ^a  

^a UNIVERSITY OF BONN   (Germany)

^b Laboratory Hansmann Weiß   (Germany)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

Complex chromosome rearrangement (CCR); Fluorescence in situ hybridization (FISH); Prenatal diagnosis; Spectral karyotyping (SKY)

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 11; CHROMOSOME 12; CHROMOSOME 13; CHROMOSOME 4; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; DEVICE; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; KARYOTYPING; MALE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SPECTROSCOPY; TWIN PREGNANCY;

ABORTION, EUGENIC; ADULT; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 4; DIAGNOSIS, DIFFERENTIAL; DISEASES IN TWINS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PREGNANCY; PREGNANCY, MULTIPLE; TWINS; ULTRASONOGRAPHY, PRENATAL;

EID: 0032730123     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199912)19:12<1143::AID-PD730>3.0.CO;2-9     Document Type: Article

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