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Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome.
Cytogenet Cell Genet. 2001;95(1-2):20-7. doi: 10.1159/000057012.
Cytogenet Cell Genet. 2001.
PMID: 11978965
Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.
DeSilva U, Elnitski L, Idol JR, Doyle JL, Gan W, Thomas JW, Schwartz S, Dietrich NL, Beckstrom-Sternberg SM, McDowell JC, Blakesley RW, Bouffard GG, Thomas PJ, Touchman JW, Miller W, Green ED.
DeSilva U, et al.
Genome Res. 2002 Jan;12(1):3-15. doi: 10.1101/gr.214802.
Genome Res. 2002.
PMID: 11779826
Free PMC article.
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