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Volumn 30, Issue 1, 2000, Pages 89-90

De novo deletion of Xq associated with premature ovarian failure

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMENORRHEA; ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DELETION X; CHROMOSOME G BAND; CHROMOSOME PAINTING; CHROMOSOME XQ; DISEASE ASSOCIATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; METAPHASE CHROMOSOME; OVARY DISEASE;

EID: 0034062680     PISSN: 00048291     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1445-5994.2000.tb01064.x     Document Type: Article
Times cited : (3)

References (9)
  • 1
    • 0031568876 scopus 로고    scopus 로고
    • Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-MB YAC contig spanning Xq21
    • 1. Sala C, Arrigo G, Torri G et al. Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-MB YAC contig spanning Xq21. Genomics 1997; 40: 123-31.
    • (1997) Genomics , vol.40 , pp. 123-131
    • Sala, C.1    Arrigo, G.2    Torri, G.3
  • 2
    • 0025092789 scopus 로고
    • The critical region on the human Xq
    • 2. Therman E, Laxova R, Susman B. The critical region on the human Xq. Hum Genet 1990; 85: 455-61.
    • (1990) Hum Genet , vol.85 , pp. 455-461
    • Therman, E.1    Laxova, R.2    Susman, B.3
  • 3
    • 0025315275 scopus 로고
    • The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: A hypothesis
    • 3. Therman E, Susman B. The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis. Hum Genet 1990; 85: 175-83.
    • (1990) Hum Genet , vol.85 , pp. 175-183
    • Therman, E.1    Susman, B.2
  • 4
    • 0028087750 scopus 로고
    • Molecular and cytogenetic studies of an X; autosome translocation in a patient with premature ovarian failure and review of the literature
    • 4. Powell CM, Taggart RT, Drumheller TC et al. Molecular and cytogenetic studies of an X; autosome translocation in a patient with premature ovarian failure and review of the literature. Am J Med Genet 1994; 52: 19-26.
    • (1994) Am J Med Genet , vol.52 , pp. 19-26
    • Powell, C.M.1    Taggart, R.T.2    Drumheller, T.C.3
  • 5
    • 0023250423 scopus 로고
    • Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome
    • 5. Krauss CM, Turksoy RN, Atkins L, McLaughlin C, Brown LG, Page DC. Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome. N Engl J Med 1987; 317: 125-31.
    • (1987) N Engl J Med , vol.317 , pp. 125-131
    • Krauss, C.M.1    Turksoy, R.N.2    Atkins, L.3    McLaughlin, C.4    Brown, L.G.5    Page, D.C.6
  • 8
    • 17344369363 scopus 로고    scopus 로고
    • A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: Evidence for conserved function in oogenesis and implications for human sterility
    • 8. Bione S, Sala C, Manzini C et al. A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility. Am J Hum Genet 1998; 62: 533-41.
    • (1998) Am J Hum Genet , vol.62 , pp. 533-541
    • Bione, S.1    Sala, C.2    Manzini, C.3
  • 9
    • 0028237295 scopus 로고
    • Obstetrical and gynecological complications in Fragile X carriers: A multicenter study
    • 9. Schwartz C, Dean J, Howard-Peebles P et al. Obstetrical and gynecological complications in Fragile X carriers: a Multicenter Study. Am J Med Genet 1994; 51: 400-2.
    • (1994) Am J Med Genet , vol.51 , pp. 400-402
    • Schwartz, C.1    Dean, J.2    Howard-Peebles, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.