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Autore Titolo Tipo [ Anno] Filtri: First Letter Of Last Name è M [Clear All Filters]
A multicenter, case-control study on risk factors for antepartum stillbirth. J Matern Fetal Neonatal Med 2011;24(3):407-10.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. Blood 2011;117(24):6673-80.
. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. Blood 2011;117(24):6673-80.
. Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2. Am J Hum Genet 2011;88(1):115-20.
. Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2. Am J Hum Genet 2011;88(1):115-20.
. Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies. Nat Genet 2011;43(3):259-63.
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