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Volumn 36, Issue 3, 1999, Pages 242-245

Triplication of distal chromosome 10q

Author keywords

Chromosome 10q; Cytogenetics; FISH; Triplication

Indexed keywords

MICROSATELLITE DNA;

EID: 0033024393     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (23)

References (14)
  • 1
    • 16944363754 scopus 로고    scopus 로고
    • Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome
    • Devriendt K, Petit P, Matthijs G, et al Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome. J Med Genet 1997;34:395-9.
    • (1997) J Med Genet , vol.34 , pp. 395-399
    • Devriendt, K.1    Petit, P.2    Matthijs, G.3
  • 2
    • 16044371402 scopus 로고    scopus 로고
    • A complete set of human telomeric probes and their clinical application
    • National Institutes of Health and Institute of Molecular Medecine Collaboration. A complete set of human telomeric probes and their clinical application. Nat Genet 1996;14:86-9.
    • (1996) Nat Genet , vol.14 , pp. 86-89
  • 3
    • 0001549979 scopus 로고
    • Chromosome 10, trisomy 10q2
    • Buyse ML, ed. Dover, USA: Blackwell Scientific Publications
    • Fryns JP. Chromosome 10, trisomy 10q2. In:Buyse ML, ed. Birth defects encyclopedia. Dover, USA: Blackwell Scientific Publications, 1990:359-60.
    • (1990) Birth Defects Encyclopedia , pp. 359-360
    • Fryns, J.P.1
  • 5
    • 0008266049 scopus 로고
    • Tetrasomy 16q12,1-q12.2 as a result of an interstitial triplication
    • Berry R, Manchester DK, Feingold M, et al. Tetrasomy 16q12,1-q12.2 as a result of an interstitial triplication. Am J Hum Genet 1990;47:A26.
    • (1990) Am J Hum Genet , vol.47
    • Berry, R.1    Manchester, D.K.2    Feingold, M.3
  • 6
    • 0008194559 scopus 로고
    • Mosaic isodicentric chromosome 9 with triplication (9p22-pter) and no deletion in an abnormal infant presenting with clinical features of trisomy 9; a new type of isodicentric chromosome formation
    • Batanian JR, Chen X, Grange DK. Mosaic isodicentric chromosome 9 with triplication (9p22-pter) and no deletion in an abnormal infant presenting with clinical features of trisomy 9; a new type of isodicentric chromosome formation. Am J Hum Genet 1994;55:A98.
    • (1994) Am J Hum Genet , vol.55
    • Batanian, J.R.1    Chen, X.2    Grange, D.K.3
  • 7
    • 0029797658 scopus 로고    scopus 로고
    • Deletion or triplication of the a3(VI) collagen gene in three patients with 2q37 chromosome aberrations and symptoms of collagen-related disorders
    • Rauch A, Pfeiffer A, Trautmann U, Deletion or triplication of the a3(VI) collagen gene in three patients with 2q37 chromosome aberrations and symptoms of collagen-related disorders. Clin Genet 1996;49:279-85.
    • (1996) Clin Genet , vol.49 , pp. 279-285
    • Rauch, A.1    Pfeiffer, A.2    Trautmann, U.3
  • 8
    • 2442752480 scopus 로고    scopus 로고
    • Partial triplication and duplication of 5p14-15.3 associated with features of trisomy 5p
    • Harrison K, Teshima I, Silver M, et al. Partial triplication and duplication of 5p14-15.3 associated with features of trisomy 5p. Am J Hum Genet 1996;59:A119.
    • (1996) Am J Hum Genet , vol.59
    • Harrison, K.1    Teshima, I.2    Silver, M.3
  • 10
    • 0000654766 scopus 로고
    • Triplication 15q 11-13 in two unrelated patients with hypotonia, cognitive delays and visual impairment
    • Holowinsky S, Black SH, Howard-Peebles PN, et al. Triplication 15q 11-13 in two unrelated patients with hypotonia, cognitive delays and visual impairment. Am J Hum Genet 1993;53:A125.
    • (1993) Am J Hum Genet , vol.53
    • Holowinsky, S.1    Black, S.H.2    Howard-Peebles, P.N.3
  • 14
    • 0029087828 scopus 로고
    • Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluoresence in situ hybridisation
    • Guo WJ, Callif-Dailey F, Zapata MC, Miller ME. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluoresence in situ hybridisation. Am J Med Genet 1995;58:230-6.
    • (1995) Am J Med Genet , vol.58 , pp. 230-236
    • Guo, W.J.1    Callif-Dailey, F.2    Zapata, M.C.3    Miller, M.E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.