Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation

American Journal of Medical Genetics

Volumn 86, Issue 2, 1999, Pages 151-155

  Van Den Berg, Cardi ^a   Pijpers, Leen ^b   Halley, Dicky J J ^a   Van Opstal, Diane ^a   Los, Frans J ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b Merwede Ziekenhuis   (Netherlands)

Author keywords

Amniotic fluid cells; DNA investigation; Fluorescence in situ hybridization; Isochromosomes 18p and 18q

Indexed keywords

AMNIOTIC FLUID CELL; ARTICLE; CASE REPORT; CHROMOSOME 18P; CHROMOSOME 18Q; CHROMOSOME ANALYSIS; DNA DETERMINATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; ISOCHROMOSOME; NEWBORN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY 18;

ADULT; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; FETAL DISEASES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; ISOCHROMOSOMES; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY;

EID: 0033543467     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990910)86:2<151::AID-AJMG12>3.0.CO;2-N     Document Type: Article

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