Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders

Fertility and Sterility

Volumn 80, Issue 4, 2003, Pages 1052-1054

  Goswami, Ravinder ^a   Goswami, Deepti ^a   Kabra, Madhulika ^a   Gupta, Nandita ^a   Dubey, Sudhisha ^a   Dadhwal, Vatsala ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

Triple X syndrome

Indexed keywords

CONJUGATED ESTROGEN; MEDROXYPROGESTERONE ACETATE; PROGESTERONE; THYROXINE;

ADULT; ARTICLE; ASPIRATION BIOPSY; CASE REPORT; CHROMOSOME BANDING PATTERN; CLINICAL FEATURE; CONGENITAL MALFORMATION; DISEASE ASSOCIATION; ECHOGRAPHY; ENCEPHALOCELE; FEMALE; GIEMSA STAIN; HASHIMOTO DISEASE; HUMAN; IDIOPATHIC THROMBOCYTOPENIC PURPURA; KARYOTYPE 47,XXX; KARYOTYPING; MAJOR CLINICAL STUDY; METAPHASE CHROMOSOME; NEWBORN; NEWBORN DEATH; PREMATURE OVARIAN FAILURE; PREMATURITY; PREVALENCE; PRIORITY JOURNAL; SECONDARY AMENORRHEA; TURNER SYNDROME;

EID: 0141889040     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0015-0282(03)01121-X     Document Type: Article

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