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Volumn 49, Issue 1, 1996, Pages 42-45

Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delay

Author keywords

FISH studies; Mild clinical features; Supernumerary marker chromosomes 6 and 9

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 6; CHROMOSOME 9; CHROMOSOME MOSAICISM; DNA PROBE; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH RETARDATION; HUMAN; HUMAN CELL; KARYOTYPE; KARYOTYPE 46,XY; LYMPHOCYTE; MALE; MARKER CHROMOSOME; PRESCHOOL CHILD; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME;

EID: 0029875791     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb04323.x     Document Type: Article
Times cited : (11)

References (13)
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  • 2
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  • 4
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    • Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes
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    • (1992) Am J Med Genet , vol.43 , pp. 709-715
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  • 6
    • 0016173775 scopus 로고
    • Bisatellited extra small metacentric chromosome in newborns
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    • Paternal isodisomy of chromosome 6 in association with a maternal supernumerary marker chromosome 6
    • James RJ, Crolla JA, Temple IK, Sitch FL, Dennis NR. Paternal isodisomy of chromosome 6 in association with a maternal supernumerary marker chromosome 6. Am J Hum Genet Suppl 1994: 55: A108.
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  • 9
    • 0027184219 scopus 로고
    • Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization
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    • Plattner, R.1    Heerema, N.A.2    Howard-Peebles, P.N.3    Miles, J.H.4    Soukup, S.5    Palmer, C.G.6
  • 10
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    • The origin of a morphologically unidentifiable human supernumerary minichromosome traced through sorting, molecular cloning and in situ hybridization
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.