DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0301_286.pdf
Reference29 articles.
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3. McLean, S.D., Saal, H.M., Spinner, N.B., Emanuel, B.S. & Driscoll, D.A. Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype. Am. J. Dis. Child. 147, 1212–1216 (1993).
4. Goodship, J., Cross, I., Scambler, P. & Burn, J. Monozygotic twins with chromosome 22q11 deletion and discordant phenotype. J. Med. Genet. 32, 746–748 (1995).
5. McDonald-McGinn, D.M. et al. The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients. Genetic Testing 1, 99–108 (1997).
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