%0 Artículo (Article) %A Ojeda D. %I Elsevier Inc. %D 2011 %G Inglés (English) %T Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype %U https://repository.urosario.edu.co/handle/10336/24059 %U https://doi.org/10.1016/j.fertnstert.2011.04.045 %X Earlier reports demonstrated a key role of Cdkn1b during mouse ovarian development. In this study, the sequencing analysis of the complete coding region of this gene in a panel of premature ovarian failure patients and control subjects reveals a novel mutation potentially related to the phenotype. © 2011 by American Society for Reproductive Medicine.