Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

Fertility and Sterility

Volumn 95, Issue 8, 2011, Pages

  Ojeda, Diego ^a   Lakhal, Besma ^b   Fonseca, Dora Janneth ^a   Braham, Rim ^b   Landolsi, Hanne ^b   Mateus, Heidi Eliana ^a   Restrepo, Carlos Martín ^a   Elghezal, Hatem ^b   Saâd, Ali ^b   Laissue, Paul ^a  

^a UNIVERSIDAD DEL ROSARIO   (Colombia)

^b FARHAT HACHED HOSPITAL   (Tunisia)

Author keywords

CDKN1B; mutations; Premature ovarian failure (POF); sequencing

Indexed keywords

CYCLIN DEPENDENT KINASE INHIBITOR 1B; FOLLITROPIN;

ADULT; ARTICLE; AUTOIMMUNE DISEASE; CONTROLLED STUDY; FEMALE; FEMALE INFERTILITY; FOLLITROPIN BLOOD LEVEL; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; HUMAN; INFORMED CONSENT; KARYOTYPE; MAJOR CLINICAL STUDY; OVARY DEVELOPMENT; OVARY INSUFFICIENCY; PELVIS SURGERY; PHENOTYPE; PREMATURE OVARIAN FAILURE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 79959751824     PISSN: 00150282     EISSN: 15565653     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2011.04.045     Document Type: Article

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