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Volumn 49, Issue 3, 1996, Pages 156-159

Jumping translocation in a phenotypically normal female

Author keywords

Chromosome 15; Chromosome 21; Chromosome mosaic; Chromosome translocation; Chromosome X; Jumping translocation; Repetitive DNA sequences

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 15; CHROMOSOME 21; CHROMOSOME MOSAICISM; CHROMOSOME TRANSLOCATION; CHROMOSOME XQ; FEMALE; HUMAN; HUMAN CELL; MALE; PERIPHERAL LYMPHOCYTE; PRIORITY JOURNAL; SKIN FIBROBLAST;

EID: 0029963913     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb03276.x     Document Type: Article
Times cited : (13)

References (12)
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  • 2
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    • Simple and nonisotopic methods to detect unknown gene mutations in nucleic acids
    • Adolph KW. ed. Orlando, Florida; Academic Press, in press
    • Bunge S, Fuchs S, Gal A. Simple and nonisotopic methods to detect unknown gene mutations in nucleic acids. In: Adolph KW. ed. Methods in molecular genetics. Orlando, Florida; Academic Press, 1996: in press.
    • (1996) Methods in Molecular Genetics
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  • 3
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    • Jumping translocation in a newborn boy with dup (4q) and severe hydrops fetalis
    • Duval E, van den Enden A, Vanhaesebrouck P, Speleman F. Jumping translocation in a newborn boy with dup (4q) and severe hydrops fetalis. Am J Med Genet 1994: 52: 214-217.
    • (1994) Am J Med Genet , vol.52 , pp. 214-217
    • Duval, E.1    Van Den Enden, A.2    Vanhaesebrouck, P.3    Speleman, F.4
  • 4
    • 0027260825 scopus 로고
    • Moving satellites and unstable chromosome translocations: Clinical and cytogenetic implications
    • Farrell SA, Winsor EJT, Markovic VD. Moving satellites and unstable chromosome translocations: clinical and cytogenetic implications. Am J Med Genet 1993: 46: 715-720.
    • (1993) Am J Med Genet , vol.46 , pp. 715-720
    • Farrell, S.A.1    Winsor, E.J.T.2    Markovic, V.D.3
  • 5
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  • 6
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    • Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion
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    • (1992) Am J Hum Genet , vol.50 , pp. 725-741
    • Giacalone, J.P.1    Francke, U.2
  • 7
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    • Molecular cytogenetic characterization of 17rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints
    • Han J-Y, Choo KHA, Shaffer LG. Molecular cytogenetic characterization of 17rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints. Am J Hum Genet 1994: 55: 969-967.
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  • 8
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    • The analysis of a long range repetitive DNA families, implications on the stability of human acrocentric chromosomes
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.