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Volumn 33, Issue SUPPL. 1, 2001, Pages

Fragile X syndrome: Premature ovarian failure, preimplantation and preconception genetic diagnosis;Síndrome del cromosoma X frágil: Menopausia precoz. Diagnóstico preimplantacional y preconcepcional

Author keywords

FMR1 gene; Fragile X syndrome; Mental retardation; Preconception genetic diagnosis; Preimplantation genetic diagnosis; Premature ovarian failure

Indexed keywords

ARTICLE; CHROMOSOME ANALYSIS; EARLY MENOPAUSE; FEMALE; FERTILIZATION IN VITRO; FRAGILE X SYNDROME; GENETIC SCREENING; HETEROZYGOTE; HUMAN; MATERNAL CARE; PREGNANCY; PREMATURE OVARIAN FAILURE; PRENATAL DIAGNOSIS; RISK FACTOR; TRINUCLEOTIDE REPEAT;

EID: 11244306162     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (8)
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  • 3
    • 0031568876 scopus 로고    scopus 로고
    • Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21
    • Sala C, Arrigo G, Torri G, Martinazzi F, Riva P, Larizza L, 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    Martinazzi, F.4    Riva, P.5    Larizza, L.6
  • 4
    • 0031857007 scopus 로고    scopus 로고
    • Studies of FRAXA and FRAXE in women with premature ovarian failure
    • Murray A, Webb J, Grimley S, Conway G, Jacobs P. Studies of FRAXA and FRAXE in women with premature ovarian failure. J Med Genet 1998; 35: 637-40.
    • (1998) J Med Genet , vol.35 , pp. 637-640
    • Murray, A.1    Webb, J.2    Grimley, S.3    Conway, G.4    Jacobs, P.5
  • 5
    • 0028025220 scopus 로고
    • Molecular analysis of the (CGG)n expansion in the FMR1 gene in 59 Spanish fragile X syndrome families
    • Milà M, Kruyer H, Glover G, Sánchez A, Carbonell P, Castellví-Bell S, et al. Molecular analysis of the (CGG)n expansion in the FMR1 gene in 59 Spanish fragile X syndrome families. Hum Genet 1994; 94: 395-400.
    • (1994) Hum Genet , vol.94 , pp. 395-400
    • Milà, M.1    Kruyer, H.2    Glover, G.3    Sánchez, A.4    Carbonell, P.5    Castellví-Bell, S.6
  • 6
    • 0029097960 scopus 로고
    • Fragile X premutations in familial premature ovarian failure
    • Conway GS, Hettiarachchi S, Murray A, Jacobs PA. Fragile X premutations in familial premature ovarian failure. Lancet 1995; 346: 309-10.
    • (1995) Lancet , vol.346 , pp. 309-310
    • Conway, G.S.1    Hettiarachchi, S.2    Murray, A.3    Jacobs, P.A.4
  • 7
    • 0033515496 scopus 로고    scopus 로고
    • Fragile X premutation is a significant risk factor for premature ovarian failure: The International Collaborative POF in Fragile X study-preliminary data
    • Allingham-Hawkins DJ, Babul-Hirji R, Chitayat D, Holden JJ, Yang KT, Lee C, et al. Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study-preliminary data. Am J Med Genet 1999; 83: 322-5.
    • (1999) Am J Med Genet , vol.83 , pp. 322-325
    • Allingham-Hawkins, D.J.1    Babul-Hirji, R.2    Chitayat, D.3    Holden, J.J.4    Yang, K.T.5    Lee, C.6
  • 8
    • 0033612244 scopus 로고    scopus 로고
    • Premature Ovarian Failure (POF) and Fragile X Premutation Females: From POF to fragile X Carrier Identification, from Fragile X carrier to POF Association Data
    • Uzielli ML, Guarducci S, Lapi E, Cecconi A, Ricci U, Ricotti G, et al. Premature Ovarian Failure (POF) and Fragile X Premutation Females: from POF to fragile X Carrier Identification, From Fragile X carrier to POF Association Data. Am J Med Genet 1999; 84: 300-3.
    • (1999) Am J Med Genet , vol.84 , pp. 300-303
    • Uzielli, M.L.1    Guarducci, S.2    Lapi, E.3    Cecconi, A.4    Ricci, U.5    Ricotti, G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.