Variable bleeding phenotype in an Amish pedigree with von Willebrand disease

Por Gupta, Sweta, Heiman, Meadow, Duncan, Natalie, Hinckley, Jesse, Di Paola, Jorge, Shapiro, Amy D
Publicado no Am J Hematol (2016)

Quantitative trait locus linkage analysis in a large Amish pedigree identifies novel candidate loci for erythrocyte traits

Por Hinckley, Jesse D, Abbott, Diana, Burns, Trudy L, Heiman, Meadow, Shapiro, Amy D, Wang, Kai, Di Paola, Jorge
Publicado em 2013

Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly

Por Fabbro, Shay, Kahr, Walter H. A., Hinckley, Jesse, Wang, Kai, Moseley, Jack, Ryu, Gi-Yung, Nixon, Brie, White, James G., Bair, Thomas, Schutte, Brian, Di Paola, Jorge
Publicado em 2011

Variable content of von Willebrand factor mutant monomer drives the phenotypic variability in a family with von Willebrand disease

Por Chen, Junmei, Hinckley, Jesse D., Haberichter, Sandra, Jacobi, Paula, Montgomery, Robert, Flood, Veronica H., Wong, Randall, Interlandi, Gianluca, Chung, Dominic W., López, José A., Di Paola, Jorge
Publicado no Blood (2015)