Gene analysis in patients with premature ovarian failure or gonadal dysgenesis: A preliminary study

Maturitas

Volumn 57, Issue 4, 2007, Pages 399-404

  Massad Costa, Ana Maria ^a   da Silva, Ismael Dale Cotrim Guerreiro ^a   Affonso, Regina ^a   Soares Jr , José Maria ^a   Nunes, Márcia Gaspar ^a   de Lima, Geraldo Rodrigues ^a   Baracat, Edmund C ^a,b  

^a FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Gene analysis; Premature ovarian failure; Pure gonadal dysgenesis; QM gene

Indexed keywords

EDETIC ACID; FOLLITROPIN;

ADULT; AMINO ACID SEQUENCE; ARTICLE; BLOOD SAMPLING; CHROMOSOME XQ; CLINICAL ARTICLE; FEMALE; FRAGILE X SYNDROME; GENE LOCATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GONADAL DYSGENESIS; HORMONE BLOOD LEVEL; HUMAN; HYPOTHESIS; KARYOTYPE 46,XX; NUCLEOTIDE SEQUENCE; OVARY INSUFFICIENCY; OVULATION; POINT MUTATION; PREMATURE OVARIAN FAILURE;

ADULT; BASE SEQUENCE; CASE-CONTROL STUDIES; FEMALE; FRAGILE X SYNDROME; GENETIC SCREENING; GONADAL DYSGENESIS, 46,XX; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; OVARIAN FAILURE, PREMATURE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RIBOSOMAL PROTEINS; TUMOR SUPPRESSOR PROTEINS;

EID: 34447252130     PISSN: 03785122     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.maturitas.2007.04.005     Document Type: Article

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