Article
Compilation of copy number variants identified in phenotypically normal and parous Japanese women.
Journal of human genetics - 1 Jun 2014
Migita Ohsuke, Maehara Kayoko, Kamura Hiromi, Miyakoshi Kei, Tanaka Mamoru, Morokuma Seiichi, Fukushima Kotaro, Shimamoto Tomihiro, Saito Shigeru, Sago Haruhiko, Nishihama Keiichiro, Abe Kosei, Nakabayashi Kazuhiko, Umezawa Akihiro, Okamura Kohji, Hata Kenichiro
Abstract excerpt
With increasing public concern about infertility and the frequent involvement of chromosomal anomalies in miscarriage, analyses of copy number variations (CNVs) have been used to identify the genomic regions responsible for each process of childbearing. Although associations between CNVs and diseases have been reported, many CNVs have also been identified in healthy individuals. Like other types of mutations,...
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