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Volumn 46, Issue 1, 2003, Pages 45-48

Pure partial trisomy 6p due to a familial insertion (16;6)(p12;p21.2p23)

Author keywords

Interchromosomal insertion; Pure 6p duplication

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 16; CHROMOSOME 6; CHROMOSOME DUPLICATION; CHROMOSOME INSERTION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INFANT; MALE; PARTIAL TRISOMY; PARTIAL TRISOMY 6P;

EID: 0038340989     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-3995(03)00004-2     Document Type: Article
Times cited : (14)

References (16)
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  • 6
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    • C.C. Morton, J.A. Brown, I.R. Kirsch, G.A. Evans, T. Mohanakumar, W.E. Nance, F.O. Redwine, J.A. Brown, Codominant expression of major histocompatibility complex (MCH) in a case of partial trisomy 6p resulting from an insertion and inversion involving heterologous chromosomes, Am J Hum Genet 32 (1980) 81A.
    • (1980) Am J Hum Genet , vol.32
    • Morton, C.C.1    Brown, J.A.2    Kirsch, I.R.3    Evans, G.A.4    Mohanakumar, T.5    Nance, W.E.6    Redwine, F.O.7    Brown, J.A.8
  • 7
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    • Detection and localization of an extra HLA locus in a karyotypically normal male by chromosomal in situ hybridization
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    • Pearson, G.1    Mann, J.D.2    Bensen, R.W.3
  • 11
    • 0344654747 scopus 로고    scopus 로고
    • "Essentially pure" Partial trisomy (6)(p23→pter) in two brothers due to maternal t(6;17)(p23;p13.3)
    • B. Röthlisberger, D. Kotzot, H.E. Gnehm, A. Schinzel, "Essentially Pure" Partial trisomy (6)(p23→pter) in two brothers due to maternal t(6;17)(p23;p13.3), Am J Med Genet 85 (1999) 389-394.
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    • Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.