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Volumn 104, Issue 3, 2001, Pages 204-208

Chromosome 10p11.2-p12.2 duplication: Report of a patient and review of the literature

Author keywords

CGH; De novo; Duplication chromosome 10p; FISH; High arched cleft palate; Mental retardation

Indexed keywords


EID: 0035576287     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.10021     Document Type: Article
Times cited : (13)

References (13)
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  • 2
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  • 3
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    • Partial duplication of the short arm of chromosome 10. Karyotype: 46, XX,dup(10p)(pter→p12::p12::p12→qter)
    • Fryns JP, Deroover J, Haegeman J, Van den Berghe H. 1979. Partial duplication of the short arm of chromosome 10. Karyotype: 46, XX,dup(10p)(pter→p12::p12::p12→qter). Hum Genet 47:217-220.
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  • 4
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  • 5
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    • Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G. 1998. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities. Ann Génét 41:133-140.
    • (1998) Ann Génét , vol.41 , pp. 133-140
    • Lapierre, J.M.1    Cacheux, V.2    Collot, N.3    Da Silva, F.4    Hervy, N.5    Rivet, D.6    Romana, S.7    Wiss, J.8    Benzaken, B.9    Aurias, A.10    Tachdjian, G.11
  • 6
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    • Deux cas de trisomie 10p partielle dus à une translocation paternelle t(10;18)(p13;p23)
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  • 7
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    • Nomoto, N.1    Nagauchi, O.2
  • 8
    • 0018168223 scopus 로고
    • The dermatoglyphic pattern of the trisomy 10p syndrome
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  • 9
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    • Romana SP, Le Coniat M, Berger R. 1994. t(12;21): a new recurrent translocation in acute lymphoblastic leukemia. Genes Chromosomes Cancer 9:186-191.
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    • Romana, S.P.1    Le Coniat, M.2    Berger, R.3
  • 12
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    • Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis
    • Stone D, Ning Y, Guan XY, Kaiser-Kupfer M, Wynshaw-Boris A, Biesecker L. 1996. Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis. Hum Genet 98:396-402.
    • (1996) Hum Genet , vol.98 , pp. 396-402
    • Stone, D.1    Ning, Y.2    Guan, X.Y.3    Kaiser-Kupfer, M.4    Wynshaw-Boris, A.5    Biesecker, L.6
  • 13
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    • Multiple abnormalities in a child with partial duplications of 10p and 13q from a 3:1 segregation of a maternal t(10;13) translocation
    • Yip MY, Williams J, Goddard A, Campbell P, Lambert I, Smithells RW. 1990. Multiple abnormalities in a child with partial duplications of 10p and 13q from a 3:1 segregation of a maternal t(10;13) translocation. J Med Genet 27:188-191.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.