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2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease.Chopra, SS, Leshchiner I., Duzkale H., McLaughlin H., Giovanni M., Zhang C., Stitziel N., Fingeroth J., Joyce RM, Lebo M., Rehm H., Vuzman D., Maas R., Sunyaev SR, Murray M., and Cassa CA Molecular genetics & genomic medicine, 2015/09/01, Volume 3, Issue 5, p.413-23, (2015) Read More / View Supplemental Materials
Abstract
Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck.Balick, DJ, Do R., Cassa CA, Reich D., and Sunyaev SR PLoS genetics, 2015/08/01, Volume 11, Issue 8, p.e1005436, (2015) Read More / View Supplemental Materials
Abstract
2013
Large Numbers of Genetic Variants Considered to be Pathogenic are Common in Asymptomatic Individuals.Cassa, CA, Tong MY, and Jordan DM Human mutation, 2013/07/01, (2013) Read More / View Supplemental Materials
Abstract
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