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Clinical Genetics|May 4, 2018
Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehogM C Digilio, F Pugnaloni, A De Luca, et al.Journal of Clinical Pharmacology|December 1, 1995
Absence of a pharmacokinetic interaction between losartan and hydrochlorothiazideJ B McCrea, M W Lo, L Tomasko, et al.Molecular Genetics and Metabolism|June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndromeA Pizzuti, G Novelli, A Ratti, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane geneG Calabrese, L Stuppia, E Morizio, et al.Human Molecular Genetics|February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeA Pizzuti, G Novelli, A Ratti, et al.Human Genetics|January 1, 1997
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A geneA Savoia, M R Piemontese, M Savino, et al.Clinical and Experimental Immunology|July 11, 2000
T cell receptor repertoire and function in patients with DiGeorge syndrome and velocardiofacial syndromeM Pierdominici, M Marziali, A Giovannetti, et al.Genomics|June 21, 2001
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunitL Berti, G Mittler, G K Przemeck, et al.Journal of Endocrinological Investigation|May 8, 2004
Evaluation of a DHPLC-based assay for rapid detection of RET germline mutations in Italian patients with medullary thyroid carcinomaI Torrente, F Arturi, L D'Aloiso, et al.Journal of Pediatric Surgery|May 11, 1999
Wilms' tumor: a 25-year review of the role of preoperative chemotherapyM L Capra, D A Walker, W M Mohammed, et al.Pageof 34