Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus [2]

Taiwanese Journal of Obstetrics and Gynecology

Volumn 46, Issue 3, 2007, Pages 284-285

  Chen, Chih Ping ^a,b   Chang, Tung Yao ^a   Liu, Yu Peng ^a   Chern, Schu Rern ^a   Wang, Wayseen ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b ASIA UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BIOMETRY; CASE REPORT; DIGYNIC TRIPLOID FETUS; DNA POLYMORPHISM; ECHOGRAPHY; FEMALE; FETUS; FETUS DISEASE; GESTATIONAL AGE; HUMAN; INTRAUTERINE GROWTH RETARDATION; KARYOTYPING; LETTER; MACROCEPHALY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRENATAL DIAGNOSIS; TRIPLOIDY;

EID: 35348918878     PISSN: 10284559     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1028-4559(08)60036-4     Document Type: Letter

References (3)

1. McFadden DE, Kalousek DK. Two different phenotypes of fetuses with chromosomal triploidy: correlation with parental origin of the extra haploid set. Am J Med Genet 1991;38:535-8.
2. McFadden DE, Kwong LC, Yam IY, Langlois S. Parental origin of triploidy in human fetuses: evidence for genomic imprinting. Hum Genet 1993;92:465-9.
3. Mittal TK, Vujanic GM, Morrissey BM, Jones A. Triploidy: antenatal sonographic features with post-mortem correlation. Prenat Diagn 1998;18:1253-62.