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Volumn 69, Issue 1, 2000, Pages 1-13

Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: The low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 5; CHROMOSOME 7Q; EVOLUTION; GENE DELETION; GENE MAPPING; HUMAN; NONHUMAN; NUCLEOTIDE REPEAT; PRIORITY JOURNAL; WILLIAMS BEUREN SYNDROME;

EID: 0034306681     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6312     Document Type: Article
Times cited : (83)

References (68)
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    • Genomic disorders: Structural features of the genome can lead to DNA rearrangements and human disease
    • (1998) Trends Genet. , vol.14 , pp. 417-422
    • Lupski, J.R.1
  • 38
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    • CYS3, a hotspot of meiotic recombination in Saccharomyces cerevisiae. Effects of heterozygosity and mismatch repair functions on gene conversion and recombination intermediates
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    • Vedel, M.1    Nicolas, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.