메뉴 건너뛰기




Volumn 112, Issue 3-4, 2006, Pages 337-340

Recombinant X chromosome in a prenatal diagnosis

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT;

EID: 32944479092     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000089890     Document Type: Article
Times cited : (3)

References (16)
  • 1
    • 0026678490 scopus 로고
    • Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
    • Allen RC, Zoghbi HY, Moseley AB, et al: Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet 51:1229-1239 (1992).
    • (1992) Am J Hum Genet , vol.51 , pp. 1229-1239
    • Allen, R.C.1    Zoghbi, H.Y.2    Moseley, A.B.3
  • 2
    • 0029591159 scopus 로고
    • Familial transmission of a duplication-deficiency X chromosome associated with partial Turner syndrome
    • Aller V, Gargallo M, Abrisqueta JA: Familial transmission of a duplication-deficiency X chromosome associated with partial Turner syndrome. Clin Genet 48:317-320 (1995).
    • (1995) Clin Genet , vol.48 , pp. 317-320
    • Aller, V.1    Gargallo, M.2    Abrisqueta, J.A.3
  • 3
    • 0034840008 scopus 로고    scopus 로고
    • Breakpoint analysis of Turner patients with partial Xp deletions: Implications for the lymphoedema gene location
    • Boucher CA, Sargent CA, Ogata T, et al: Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location. J Med Genet 38:591-598 (2001).
    • (2001) J Med Genet , vol.38 , pp. 591-598
    • Boucher, C.A.1    Sargent, C.A.2    Ogata, T.3
  • 4
    • 0019517904 scopus 로고
    • Phenotypically normal individuals with an inversion (X)(p22q13) and the recombinant (X),dup q
    • Buckton KE, Newton MS, Collyer S, et al: Phenotypically normal individuals with an inversion (X)(p22q13) and the recombinant (X),dup q. Ann Hum Genet 45:159-168 (1981).
    • (1981) Ann Hum Genet , vol.45 , pp. 159-168
    • Buckton, K.E.1    Newton, M.S.2    Collyer, S.3
  • 5
    • 0038462118 scopus 로고    scopus 로고
    • Prenatal diagnosis of de novo partial trisomy Xq (Xq22.1→qter) and terminal Xp deletion following sonographic detection of intrauterine growth restriction
    • Chen CP: Prenatal diagnosis of de novo partial trisomy Xq (Xq22.1→qter) and terminal Xp deletion following sonographic detection of intrauterine growth restriction. Prenat Diagn 23:518-519 (2003).
    • (2003) Prenat Diagn , vol.23 , pp. 518-519
    • Chen, C.P.1
  • 6
    • 0023780304 scopus 로고
    • A recombinant X chromosome in a short statured girl resulting from a maternal pericentric inversion
    • Duckett DP, Young ID: A recombinant X chromosome in a short statured girl resulting from a maternal pericentric inversion. Hum Genet 79:251-254 (1988).
    • (1988) Hum Genet , vol.79 , pp. 251-254
    • Duckett, D.P.1    Young, I.D.2
  • 7
    • 0031798509 scopus 로고    scopus 로고
    • A study of females with deletions of the short arm of the X chromosome
    • James RS, Coppin B, Dalton P, et al: A study of females with deletions of the short arm of the X chromosome. Hum Genet 102:507-516 (1998).
    • (1998) Hum Genet , vol.102 , pp. 507-516
    • James, R.S.1    Coppin, B.2    Dalton, P.3
  • 8
    • 0026495364 scopus 로고
    • Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
    • Kallioniemi A, Kallioniemi OP, Sudar D, et al: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258:818-821 (1992).
    • (1992) Science , vol.258 , pp. 818-821
    • Kallioniemi, A.1    Kallioniemi, O.P.2    Sudar, D.3
  • 10
    • 0016409479 scopus 로고
    • Four new cases of X-autosome translocation in man
    • author's translation
    • Laurent C, Biemont MC, Dutrillaux B: Four new cases of X-autosome translocation in man (author's translation). Humangenetik 26:35-46 (1975).
    • (1975) Humangenetik , vol.26 , pp. 35-46
    • Laurent, C.1    Biemont, M.C.2    Dutrillaux, B.3
  • 11
    • 0018341850 scopus 로고
    • Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome
    • Maeda T, Ohno M, Takada M, et al: Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome. Clin Genet 15:259-266 (1979).
    • (1979) Clin Genet , vol.15 , pp. 259-266
    • Maeda, T.1    Ohno, M.2    Takada, M.3
  • 12
    • 0019956348 scopus 로고
    • Partial Turner's syndrome in four girls with Xq duplication and Xp deficiency
    • Nielsen LB, Boczkowski K, Mikkelsen M, et al: Partial Turner's syndrome in four girls with Xq duplication and Xp deficiency. Hum Genet 61:12-17 (1982).
    • (1982) Hum Genet , vol.61 , pp. 12-17
    • Nielsen, L.B.1    Boczkowski, K.2    Mikkelsen, M.3
  • 13
    • 0033846539 scopus 로고    scopus 로고
    • The Turner syndrome-associated neurocognitive phenotype maps to distal Xp
    • Ross JL, Roeltgen D, Kushner H, et al: The Turner syndrome-associated neurocognitive phenotype maps to distal Xp. Am J Hum Genet 67:672-681 (2000).
    • (2000) Am J Hum Genet , vol.67 , pp. 672-681
    • Ross, J.L.1    Roeltgen, D.2    Kushner, H.3
  • 14
    • 0018825804 scopus 로고
    • A duplication-deficiency X chromosome in a girl with severe mental retardation
    • Sacchi N, Dalpra L, Kehyayan E: A duplication-deficiency X chromosome in a girl with severe mental retardation. Hum Genet 54:279-281 (1980).
    • (1980) Hum Genet , vol.54 , pp. 279-281
    • Sacchi, N.1    Dalpra, L.2    Kehyayan, E.3
  • 15
  • 16
    • 0032471420 scopus 로고    scopus 로고
    • Evidence for a Turner syndrome locus or loci at Xp 11.2→p22.1
    • Zinn AR, Tonk VS, Chen Z, et al: Evidence for a Turner syndrome locus or loci at Xp 11.2→p22.1. Am J Hum Genet 63:1757-1766 (1998).
    • (1998) Am J Hum Genet , vol.63 , pp. 1757-1766
    • Zinn, A.R.1    Tonk, V.S.2    Chen, Z.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.