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Archives of Gynecology and Obstetrics
Volumn 267, Issue 3, 2003, Pages 173-174
Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter→q22:)
Author keywords

Fluorescein in situ hybridization; Gonadal dysgenesis; Mayer Rokitansky Kuster Hauser syndrome; Xq deletion
Indexed keywords

ADULT; AMENORRHEA; ARTICLE; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME XQ; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE DUPLICATION; GENE PROBE; GONADAL DYSGENESIS; HUMAN; KARYOTYPE; OVARY DEVELOPMENT; ROKITANSKY SYNDROME; CHROMOSOME DELETION; CONGENITAL MALFORMATION; GENETICS; KARYOTYPING; OVARY; SYNDROME; UTERUS; X CHROMOSOME;
EID: 0037839060     PISSN: 09320067     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00404-001-0274-3     Document Type: Article
Times cited : (24)
References (14)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.