CATCH 22 (Chromosome 22q11 Deletion Syndrome)
Author:
Aldinger Kimberly
Publisher
Springer New York
Reference25 articles.
1. Augusseau, S., Jouk, S., Jalbert, P., & Prieur, M. (1986). DiGeorge syndrome and 22q11 rearrangements. Human Genetics, 74, 206. 2. Botto, L. D., May, K., Fernhoff, P. M., Correa, A., Coleman, K., Rasmussen, S. A., Merritt, R. K., O’Leary, L. A., Wong, L. Y., Elixson, E. M., Mahle, W. T., & Campbell, R. M. (2003). A population-based study of the 22q11.2 deletion: Phenotype, incidence, and contribution to major birth defects in the population. Pediatrics, 112, 101–107. 3. Burn, J. (1999). Closing time for CATCH22. Journal of Medical Genetics, 36, 737–738. 4. Burn, J., Takao, A., Wilson, D., Cross, I., Momma, K., Wadey, R., Scambler, P., & Goodship, J. (1993). Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11. Journal of Medical Genetics, 30(10), 822–824. 5. Cohen, E., Chow, E. W., Weksberg, R., & Bassett, A. S. (1999). Phenotype of adults with the 22q11 deletion syndrome: A review. American Journal of Medical Genetics, 86, 359–365.
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