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Volumn 73, Issue 9, 2006, Pages 840-842

Unbalanced X; Autosome translocation

Author keywords

Autosome translocation; Mental retardation; Monosomy 14q11.2; Monosomy Xq28; X

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 14Q; CHROMOSOME ANALYSIS; CHROMOSOME SEGREGATION; CHROMOSOME TRANSLOCATION; CHROMOSOME TRANSLOCATION X|AUTOSOME; CHROMOSOME XQ; CORPUS CALLOSUM AGENESIS; DEVELOPMENTAL DISORDER; FACE DYSMORPHIA; FEMALE; HUMAN; INFANT; MENTAL DEFICIENCY; MICROCEPHALY; SEIZURE; SPASTICITY; X CHROMOSOME;

EID: 33749482195     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02790399     Document Type: Article
Times cited : (19)

References (9)
  • 1
    • 0036898950 scopus 로고    scopus 로고
    • Molecular cytogenetic analysis of the spreading of X inactivation in X; autosome translocations
    • Sharp AJ, Spotswood HT, Robinson DO, Turner BM. Jacobs PA. Molecular cytogenetic analysis of the spreading of X inactivation in X; autosome translocations. Hum Mol Gen 2002; 11 : 3145-3156.
    • (2002) Hum Mol Gen , vol.11 , pp. 3145-3156
    • Sharp, A.J.1    Spotswood, H.T.2    Robinson, D.O.3    Turner, B.M.4    Jacobs, P.A.5
  • 2
    • 0036898974 scopus 로고    scopus 로고
    • Unbalanced X; autosome translocations provide evidence for sequence specificity in the association of XIST RNA chromatin
    • Hall L L, Christine M C, Bryon M, Wydner K, Lawrence J B. Unbalanced X; autosome translocations provide evidence for sequence specificity in the association of XIST RNA chromatin. Hum Mol Gen 2002; 11 : 3157-3165.
    • (2002) Hum Mol Gen , vol.11 , pp. 3157-3165
    • Hall, L.L.1    Christine, M.C.2    Bryon, M.3    Wydner, K.4    Lawrence, J.B.5
  • 3
    • 0017223853 scopus 로고
    • Mammalian X chromosome inactivation
    • Gartler SM, Andina RK. Mammalian X chromosome inactivation. Adv Hum Genet 1976; 7 : 99-140.
    • (1976) Adv Hum Genet , vol.7 , pp. 99-140
    • Gartler, S.M.1    Andina, R.K.2
  • 8
    • 0000781807 scopus 로고
    • Holoprosencephaly associated with 46, XX, del (14) (q11.1q13)
    • Proc 8th Int Congr Hum Genet, abst 1483
    • Levin SW, Surana RB. Holoprosencephaly associated with 46, XX, del (14) (q11.1q13). Proc 8th Int Congr Hum Genet, abst 1483. Am J Hum Genet Suppl 1991; 49 : 269.
    • (1991) Am J Hum Genet Suppl , vol.49 , pp. 269
    • Levin, S.W.1    Surana, R.B.2
  • 9
    • 0029846092 scopus 로고    scopus 로고
    • De novo interstitial proximal deletion of 14q and prenatal diagnosis of holoprosencephaly
    • Bruyere H, Favre B, Douvier S, Nivelon-Chevalier A, Mugneret F. De novo interstitial proximal deletion of 14q and prenatal diagnosis of holoprosencephaly. Prenat Diagn 1996; 16 : 1059-1060.
    • (1996) Prenat Diagn , vol.16 , pp. 1059-1060
    • Bruyere, H.1    Favre, B.2    Douvier, S.3    Nivelon-Chevalier, A.4    Mugneret, F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.