Additional genomic duplications in AZFc underlie the b2/b3 deletion-associated risk of spermatogenic impairment in Han Chinese population

Gene copy number reduction in the azoospermia factor c (AZFc) region and its effect on total motile sperm count

(2011) Michiel J. Noordam et al.   HUMAN MOLECULAR GENETICS

Structural variation of the human genome: mechanisms, assays, and role in male infertility

(2011) Claudia M.B. Carvalho et al.   Systems Biology in Reproductive Medicine

The AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertility

(2010) P. Navarro-Costa et al.   HUMAN REPRODUCTION UPDATE

Copy Number Variation in Human Health, Disease, and Evolution

(2009) Feng Zhang et al.   Annual Review of Genomics and Human Genetics

Partial AZFc deletions and duplications: clinical correlates in the Italian population

(2008) Claudia Giachini et al.   HUMAN GENETICS

The b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese population

(2008) C. Lu et al.   HUMAN MOLECULAR GENETICS

A Frequent Partial AZFc Deletion does not Render an Increased Risk of Spermatogenic Impairment in East Asians

(2005) F. Zhang et al.   ANNALS OF HUMAN GENETICS