메뉴 건너뛰기




Volumn 92, Issue 2, 2009, Pages 828.e3-828.e6

Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure

Author keywords

comparative genomic hybridization; fluorescent in situ hybridization; Premature ovarian failure; X Y translocation

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME TRANSLOCATION X; CHROMOSOME TRANSLOCATION Y; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; KARYOTYPING; POLYMERASE CHAIN REACTION; PREMATURE OVARIAN FAILURE; PRIORITY JOURNAL; RARE DISEASE;

EID: 67651085298     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2008.07.014     Document Type: Article
Times cited : (8)

References (13)
  • 2
    • 0034065580 scopus 로고    scopus 로고
    • Mapping of the POF1 locus and identification of putative genes for premature ovarian failure
    • Davisen R.M., Fox M., and Conway G.S. Mapping of the POF1 locus and identification of putative genes for premature ovarian failure. Mol Hum Reprod 6 (2000) 314-318
    • (2000) Mol Hum Reprod , vol.6 , pp. 314-318
    • Davisen, R.M.1    Fox, M.2    Conway, G.S.3
  • 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 40 (1997) 123-131
    • (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
    • 0742288906 scopus 로고    scopus 로고
    • Genetic changes in human fetuses from spontaneous abortion after in vitro fertilization detected by comparative genomic hybridization
    • Tan Y.Q., Hu L., Lin G., Sham J.S.T., Gong F., Guan X.Y., et al. Genetic changes in human fetuses from spontaneous abortion after in vitro fertilization detected by comparative genomic hybridization. Biol Reprod 70 (2004) 495-499
    • (2004) Biol Reprod , vol.70 , pp. 495-499
    • Tan, Y.Q.1    Hu, L.2    Lin, G.3    Sham, J.S.T.4    Gong, F.5    Guan, X.Y.6
  • 5
    • 0031137667 scopus 로고    scopus 로고
    • Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X:Y translocation in a patient with secondary amenorrhoea
    • Delon B., Lallaoui H., Abel-Lablanche C., Geneix A., Bellec V., and Benkhalifa M. Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X:Y translocation in a patient with secondary amenorrhoea. Mol Hum Reprod 3 (1997) 439-443
    • (1997) Mol Hum Reprod , vol.3 , pp. 439-443
    • Delon, B.1    Lallaoui, H.2    Abel-Lablanche, C.3    Geneix, A.4    Bellec, V.5    Benkhalifa, M.6
  • 6
    • 0023250423 scopus 로고
    • Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome
    • Krauss C.M., Turksoy R.N., Atkins L., McLaughlin C., Brown L.G., and Page D.C. Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome. N Engl J Med 317 (1987) 125-131
    • (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
  • 7
    • 0027440971 scopus 로고
    • Deletion (X) (q26.1→q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions
    • Tharapel A.T., Anderson K.P., Simpson J.L., Martens P.R., Wilroy Jr. R.S., Llerena Jr. J.C., et al. Deletion (X) (q26.1→q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions. Am J Hum Genet 52 (1993) 463-471
    • (1993) Am J Hum Genet , vol.52 , pp. 463-471
    • Tharapel, A.T.1    Anderson, K.P.2    Simpson, J.L.3    Martens, P.R.4    Wilroy Jr., R.S.5    Llerena Jr., J.C.6
  • 8
    • 0032959540 scopus 로고    scopus 로고
    • Risk of gonadoblastoma in female patients with Y chromosome abnormalities and dysgenetic gonads
    • Gibbons B., Tan S.Y., Yu C.C., Cheah E., and Tan H.L. Risk of gonadoblastoma in female patients with Y chromosome abnormalities and dysgenetic gonads. J Paediatr Child Health 35 (1999) 210-213
    • (1999) J Paediatr Child Health , vol.35 , pp. 210-213
    • Gibbons, B.1    Tan, S.Y.2    Yu, C.C.3    Cheah, E.4    Tan, H.L.5
  • 9
    • 0023551765 scopus 로고
    • Hypothesis: a Y-chromosomal gene causes gonadoblastoma in dysgenetic gonads
    • Page D.C. Hypothesis: a Y-chromosomal gene causes gonadoblastoma in dysgenetic gonads. Development 101 Suppl. (1987) 151-155
    • (1987) Development , vol.101 , Issue.SUPPL , pp. 151-155
    • Page, D.C.1
  • 10
    • 0028807452 scopus 로고
    • Gonadoblastoma: molecular definition of the susceptibility region on the Y chromosome
    • Tsuchiya K., Reijo R., Page D.C., and Disteche C.M. Gonadoblastoma: molecular definition of the susceptibility region on the Y chromosome. Am J Hum Genet 57 (1995) 1400-1407
    • (1995) Am J Hum Genet , vol.57 , pp. 1400-1407
    • Tsuchiya, K.1    Reijo, R.2    Page, D.C.3    Disteche, C.M.4
  • 11
    • 0034488388 scopus 로고    scopus 로고
    • Expression of a candidate gene for the gonadoblastoma locus in gonadoblastoma and testicular seminoma
    • Lau Y., Chou P., Iezzoni J., Alonzo J., and Kömüves L. Expression of a candidate gene for the gonadoblastoma locus in gonadoblastoma and testicular seminoma. Cytogenet Cell Genet 91 (2000) 160-164
    • (2000) Cytogenet Cell Genet , vol.91 , pp. 160-164
    • Lau, Y.1    Chou, P.2    Iezzoni, J.3    Alonzo, J.4    Kömüves, L.5
  • 12
    • 0033709679 scopus 로고    scopus 로고
    • Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material: a population study
    • Gravholt C.H., Fedder J., Naeraa R.W., and Muller J. Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material: a population study. J Clin Endocrinol Metab 85 (2000) 3199-3202
    • (2000) J Clin Endocrinol Metab , vol.85 , pp. 3199-3202
    • Gravholt, C.H.1    Fedder, J.2    Naeraa, R.W.3    Muller, J.4
  • 13
    • 33750309135 scopus 로고    scopus 로고
    • Detection of hidden Y mosaicism in Turner's syndrome: importance in the prevention of gonadoblastoma
    • Bianco B., Lipay M.V., Melaragno M.I., Guedes A.D., and Verreschi I.T. Detection of hidden Y mosaicism in Turner's syndrome: importance in the prevention of gonadoblastoma. J Pediatr Endocrinol Metab 19 (2006) 1113-1117
    • (2006) J Pediatr Endocrinol Metab , vol.19 , pp. 1113-1117
    • Bianco, B.1    Lipay, M.V.2    Melaragno, M.I.3    Guedes, A.D.4    Verreschi, I.T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.