Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q)

Prenatal Diagnosis

Volumn 16, Issue 11, 1996, Pages 1046-1050

  Mercier, S ^a,b   Fellmann, F ^b   Cattin, J ^c   Bresson, J L ^b  

^a CNRS   (France)

^b Lab Physiologie et Pharmacologie   (France)

^c Cabinet d'Echographie   (France)

Author keywords

Complex chromosomal rearrangement; De novo; Fluorescence in situ hybridization; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; FEMALE; FETUS; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; INFANT; NEWBORN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADULT; AMNIOCENTESIS; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 3; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; GESTATIONAL AGE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PREGNANCY; PRENATAL DIAGNOSIS; ULTRASONOGRAPHY, PRENATAL;

EID: 0029811054     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199611)16:11<1046::AID-PD989>3.0.CO;2-O     Document Type: Article

References (13)

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