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Prenatal Diagnosis

Volumn 20, Issue 9, 2000, Pages 750-753

Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

(6) Chen, Chih Ping a,b Chern, Schu Rern b Yeh, Li Fan a Chen, Wen Lin a Chen, Li Feng a Wang, Wayseen b

a MACKAY MEMORIAL HOSPITAL (Taiwan)

b NATIONAL YANG MING UNIVERSITY (Taiwan)

Author keywords

Double trisomy; Enlarged cisterna magna; Meiosis II non disjunction; Trisomy 18; Trisomy X

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 18; FEMALE; FETUS ECHOGRAPHY; GENETIC ANALYSIS; GENETIC COUNSELING; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY; X CHROMOSOME;

ADULT; CASE REPORT; CHROMOSOMES, HUMAN, PAIR 18; CISTERNA MAGNA; DNA; FEMALE; FETAL BLOOD; FETAL GROWTH RETARDATION; FLUORESCENCE; HEART SEPTAL DEFECTS, VENTRICULAR; HUMAN; KARYOTYPING; MALE; MICROSATELLITE REPEATS; POLYHYDRAMNIOS; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATIONS; SUPPORT, NON-U.S. GOV'T; TRISOMY; X CHROMOSOME;

EID: 0033806611 PISSN: 01973851 EISSN: None Source Type: Journal
DOI: 10.1002/1097-0223(200009)20:9<750::AID-PD900>3.0.CO;2-E Document Type: Article

Times cited : (22)

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