Prenatal diagnosis of trisomy 9: Cytogenetic, fish, and DNA studies

Prenatal Diagnosis

Volumn 17, Issue 10, 1997, Pages 933-940

  Van Den Berg, Cardi ^a   Ramlakhan, Sarvan K ^a   Van Opstal, Diane ^a   Brandenburg, Helen ^a   Halley, Dicky J J ^a   Los, Frans J ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

Amniotic fluid; Chorionic villi; Mosaicism; Trisomy 9; Uniparental disomy

Indexed keywords

AMNION FLUID ANALYSIS; ARTICLE; CHROMOSOME 9; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CYTOGENETICS; DIAGNOSTIC ACCURACY; DNA DETERMINATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; HUMAN; MOSAICISM; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME; TRISOMY;

ALLELES; AMNIOTIC FLUID; CHORIONIC VILLI; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; FOLLOW-UP STUDIES; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MICROSATELLITE REPEATS; POLYMERASE CHAIN REACTION; PREGNANCY; PREGNANCY OUTCOME; PROSPECTIVE STUDIES; ULTRASONOGRAPHY, PRENATAL;

EID: 0030833320     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199710)17:10<933::AID-PD179>3.0.CO;2-0     Document Type: Article

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