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Volumn 85, Issue 2, 1999, Pages 117-122

Ring 2 chromosome: Ten-year follow-up report

Author keywords

Deletion 2q; General ring syndrome; Intrauterine growth retardation; Postnatal growth retardation; Ring 2 chromosome; Silver Russell syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; GENE DELETION; GROWTH DISORDER; GROWTH RETARDATION; HUMAN; HUMAN CELL; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; RING CHROMOSOME; SILVER RUSSELL SYNDROME;

EID: 0032998002     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990716)85:2<117::AID-AJMG4>3.0.CO;2-O     Document Type: Article
Times cited : (15)

References (14)
  • 2
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    • Côté GB, Katsantoni A, Deligeorgis D. 1981. The cytogenetic and clinical implication of a ring 2 chromosome. Ann Genet 24:231-235.
    • (1981) Ann Genet , vol.24 , pp. 231-235
    • Côté, G.B.1    Katsantoni, A.2    Deligeorgis, D.3
  • 4
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    • In tema di patologia autosomica: Sindrome plurimalformativa con cromosoma ad anello del gruppo A
    • Garau A, Crisponi G, Cossu P. 1973. In tema di patologia autosomica: sindrome plurimalformativa con cromosoma ad anello del gruppo A. Clin Pediatr (Parma) 55:84-95.
    • (1973) Clin Pediatr (Parma) , vol.55 , pp. 84-95
    • Garau, A.1    Crisponi, G.2    Cossu, P.3
  • 6
    • 0023153582 scopus 로고
    • Does a "ring syndrome" exists? An analysis of 207 case reports on patients with a ring autosome
    • Kosztolányi G. 1987. Does a "ring syndrome" exists? An analysis of 207 case reports on patients with a ring autosome. Hum Genet 75:174-179.
    • (1987) Hum Genet , vol.75 , pp. 174-179
    • Kosztolányi, G.1
  • 7
    • 0018324976 scopus 로고
    • Three cases of ring chromosome 2, one derived from a paternal 2/6 translocation
    • Maraschio P, Danesino C, Garau A, Saputo V, Vigi V, Volpato S. 1979. Three cases of ring chromosome 2, one derived from a paternal 2/6 translocation. Hum Genet 48:157-167.
    • (1979) Hum Genet , vol.48 , pp. 157-167
    • Maraschio, P.1    Danesino, C.2    Garau, A.3    Saputo, V.4    Vigi, V.5    Volpato, S.6
  • 10
    • 0030916590 scopus 로고    scopus 로고
    • RDCI, the vasoactive intestinal peptide receptor: A candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37
    • Power MM, James RS, Barber JC, Fisher AM, Wood PJ, Leatherdale BA, Flanagan DE, Hatchwell E. 1997. RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37. J Med Genet 34:287-290.
    • (1997) J Med Genet , vol.34 , pp. 287-290
    • Power, M.M.1    James, R.S.2    Barber, J.C.3    Fisher, A.M.4    Wood, P.J.5    Leatherdale, B.A.6    Flanagan, D.E.7    Hatchwell, E.8
  • 11
    • 0018172172 scopus 로고
    • 46,XX/46,XX,r(2)(p25q37) Mosaicism: Clinical and cytogenetic studies
    • Sutherland GR, Carter RF. 1978. 46,XX/46,XX,r(2)(p25q37) Mosaicism: clinical and cytogenetic studies. Ann Genet 21:164-167.
    • (1978) Ann Genet , vol.21 , pp. 164-167
    • Sutherland, G.R.1    Carter, R.F.2
  • 12
    • 0019165943 scopus 로고
    • Ring chromosome 2 in a child with growth failure and few congenital abnormalities
    • Vigfusson NV, Kapstater KJ, Lloyd MA. 1980. Ring chromosome 2 in a child with growth failure and few congenital abnormalities. Am J Med Genet 7:383-389.
    • (1980) Am J Med Genet , vol.7 , pp. 383-389
    • Vigfusson, N.V.1    Kapstater, K.J.2    Lloyd, M.A.3
  • 13
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    • Human chromosome 2 rod/ring mosaicism: Probable origin by prezygotic breakage and intrachromosomal exchange
    • Wyandt HE, Kasprzak R, Lamb A, Willson K, Wilson WG, Kelly TE. 1982. Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchange. Cell Genetics 33:222-231.
    • (1982) Cell Genetics , vol.33 , pp. 222-231
    • Wyandt, H.E.1    Kasprzak, R.2    Lamb, A.3    Willson, K.4    Wilson, W.G.5    Kelly, T.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.