The genomic basis of the β-subunit of human chorionic gonadotropin diversity in triploidy
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference5 articles.
1. Placental insufficiency as a possible cause of low maternal serum human chorionic gonadotropin and low maternal serum unconjugated estriol levels in triploidy;Fejgin;AM J OBSTET GYNECOL,1993
2. Two different types of fetuses with chromosomal triploidy: correlation with parental origin of the extra haploid set;McFadden;Am J Hum Genet,1991
3. Genomic imprinting, human chorionic gonadotropin, and triploidy;Haig;Prenat Diagn,1993
4. Genomic imprinting: review and relevance to human diseases;Hall;Am J Hum Genet,1990
5. Parental imprinting of the human H19 gene;Rachmilewitz;FEBS Lett,1992
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