QuickView for FAM9A;jsessionid=AD65C3EB86F0F0468439D279AB974EB3 (gene)

1. Scrutinizing the human TEX genes in the context of human male infertility.
2. Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiet…
3. Novel interstitial deletion in Xp22.3 in a typical X-linked recessive family with Kallmann syndrome.
4. A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications…
5. Disease-dependent differently methylated regions (D-DMRs) of DNA are enriched on the X chromosome in…

There were no clinical trials for FAM9A;jsessionid=AD65C3EB86F0F0468439D279AB974EB3