Titolo | Pubblicato in | Anno |
---|---|---|
Integration of Omics Data in Genetic Epidemiology | HUMAN HEREDITY | 2015 |
Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease | GASTROENTEROLOGY | 2015 |
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome | AMERICAN JOURNAL OF HUMAN GENETICS | 2015 |
Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions | HUMAN REPRODUCTION | 2015 |
A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report | BMC GASTROENTEROLOGY | 2015 |
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