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Volumn 6, Issue 4, 1997, Pages 341-345

Are t(X;Y) (p22;q11) translocations in females frequently associated with Madelung deformity?

Author keywords

Madelung deformity; X, Y translocation

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME MAP; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; DYSCHONDROSTEOSIS; FEMALE; HUMAN; KARYOTYPE; PRIORITY JOURNAL; SHORT STATURE; TURNER SYNDROME;

EID: 0030765593     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199710000-00007     Document Type: Article
Times cited : (18)

References (14)
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    • Barbaux S, Vilain E, Raoul O, Gilgenkrantz S, Jeandidier E, Chadena D, Souleyreau N, Fellous M, McElreavey K (1995): Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata. Hum Mol Genet 4: 1565-1568.
    • (1995) Hum Mol Genet , vol.4 , pp. 1565-1568
    • Barbaux, S.1    Vilain, E.2    Raoul, O.3    Gilgenkrantz, S.4    Jeandidier, E.5    Chadena, D.6    Souleyreau, N.7    Fellous, M.8    McElreavey, K.9
  • 3
    • 0015939269 scopus 로고
    • Y to X translocation in a woman with reproductive failure
    • Khudr G, Benirschke K, Judd HL, Strauss J (1973): Y to X translocation in a woman with reproductive failure. JAMA 226: 544-549.
    • (1973) JAMA , vol.226 , pp. 544-549
    • Khudr, G.1    Benirschke, K.2    Judd, H.L.3    Strauss, J.4
  • 4
    • 0023242425 scopus 로고
    • An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences Application to Hemophilia A
    • Kogan SC, Doherty M, Gitschier J (1987): An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences Application to Hemophilia A. N Engl J Med 317: 985-990.
    • (1987) N Engl J Med , vol.317 , pp. 985-990
    • Kogan, S.C.1    Doherty, M.2    Gitschier, J.3
  • 7
    • 0025970931 scopus 로고
    • A human X-Y homologous regions encodes "amelogenin"
    • Nakahori Y, Takenaka O, Nakagome Y (1991): A human X-Y homologous regions encodes "amelogenin". Genomics 9: 264-269.
    • (1991) Genomics , vol.9 , pp. 264-269
    • Nakahori, Y.1    Takenaka, O.2    Nakagome, Y.3
  • 8
    • 0029021639 scopus 로고
    • Turner syndrome and female sex chromosome aberrations: Deduction of the principal factors involved in the development of clinical features
    • Ogata T, Matsuo N (1995): Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features. Hum Genet 95: 607-629.
    • (1995) Hum Genet , vol.95 , pp. 607-629
    • Ogata, T.1    Matsuo, N.2
  • 10
    • 0018868560 scopus 로고
    • Observations in a case of an X/Y translocation, t(X;Y) (p22;q11) in a mother and son
    • Pfeiffer RA (1980): Observations in a case of an X/Y translocation, t(X;Y) (p22;q11) in a mother and son. Cytogenet Cell Genet 26: 150-157.
    • (1980) Cytogenet Cell Genet , vol.26 , pp. 150-157
    • Pfeiffer, R.A.1
  • 12
    • 0021795677 scopus 로고
    • Detection at amniocentesis of a maternally inherited X;Y translocation
    • Speevak M, Clifford B, Cox DM, Hunter AGW (1985): Detection at amniocentesis of a maternally inherited X;Y translocation. Clin Genet 27: 595-599.
    • (1985) Clin Genet , vol.27 , pp. 595-599
    • Speevak, M.1    Clifford, B.2    Cox, D.M.3    Hunter, A.G.W.4
  • 14
    • 0020084308 scopus 로고
    • Cytogenetic studies in a Y to X translocation observed in three members of one family, with evidence of infertility in male carriers
    • Yamada K, Nanko S, Hattori S, Isurugi K (1992): Cytogenetic studies in a Y to X translocation observed in three members of one family, with evidence of infertility in male carriers. Hum Genet 60: 85-90.
    • (1992) Hum Genet , vol.60 , pp. 85-90
    • Yamada, K.1    Nanko, S.2    Hattori, S.3    Isurugi, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.