Early prenatal diagnosis of triploidy
- 31 March 1997
- journal article
- Published by Elsevier in American Journal of Obstetrics and Gynecology
- Vol. 176 (3) , 550-554
- https://doi.org/10.1016/s0002-9378(97)70546-5
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Prenatal diagnosis of triploidy during the second trimester of pregnancyPublished by Wolters Kluwer Health ,1999
- Partial mole and triploidy: Screening patients with first-trimester spontaneous abortionObstetrics & Gynecology, 1996
- Crown-rump length in chromosomally abnormal fetuses at 10 to 13 weeks' gestationAmerican Journal of Obstetrics and Gynecology, 1995
- Fetal nuchal translucency: ultrasound screening for fetal trisomy in the first trimester of pregnancyBJOG: An International Journal of Obstetrics and Gynaecology, 1994
- Maternal serum screening and triploidyPrenatal Diagnosis, 1994
- Parental origin of triploidy in human fetuses: evidence for genomic imprintingHuman Genetics, 1993
- Placental insufficiency as a possible cause of low maternal serum human chorionic gonadotropin and low maternal serum unconjugated estriol levels in triploidyAmerican Journal of Obstetrics and Gynecology, 1992
- Two different phenotypes of fetuses with chromosomal triploidy: Correlation with parental origin of the extra haploid setAmerican Journal of Medical Genetics, 1991
- Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative european study on 52 965 amniocentesesPrenatal Diagnosis, 1984
- Human triploidy: relationship between parental origin of the additional haploid complement and development of partial hydatidiform moleAnnals of Human Genetics, 1982