The genomic basis of the β-subunit of human chorionic gonadotropin diversity in triploidy
- 1 February 1994
- journal article
- Published by Elsevier in American Journal of Obstetrics and Gynecology
- Vol. 170 (2) , 700-701
- https://doi.org/10.1016/s0002-9378(94)70254-3
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Genomic imprinting, human chorionic gonadotropin, and triploidyPrenatal Diagnosis, 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
- Parental imprinting of the human H19 geneFEBS Letters, 1992
- Two different phenotypes of fetuses with chromosomal triploidy: Correlation with parental origin of the extra haploid setAmerican Journal of Medical Genetics, 1991