(2011). Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype.
Chicago Style (17th ed.) CitationSequence Analysis of the CDKN1B Gene in Patients with Premature Ovarian Failure Reveals a Novel Mutation Potentially Related to the Phenotype. 2011.
MLA (8th ed.) CitationSequence Analysis of the CDKN1B Gene in Patients with Premature Ovarian Failure Reveals a Novel Mutation Potentially Related to the Phenotype. 2011.
Warning: These citations may not always be 100% accurate.