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X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells 2018 Ho, Bianca; Greenlaw, Keelin; Al Tuwaijri, Abeer; Moussette, Sanny; Martínez, Francisco; Giorgio, Elisa; Brusco, Alfredo; Ferrero, Giovanni Battista; Linhares, Natália D; Valadares, Eugênia R; Svartman, Marta; Kalscheuer, Vera M; Rodríguez Criado, Germán; Laprise, Catherine; Greenwood, Celia M T; Naumova, Anna K
X Cittadino 2010 Ljiljana Banjanin
X Congresso della FIEC (Québec, 23-27 Agosto 1994) 1995 E. MALASPINA
X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred 1996 MacKenzie JJ; Fitzpatrick J; Babyn P; Ferrero GB; Ballabio A; Billingsley G; Bulman DE; Strasberg P; Ray PN; Costa T.
X-chromosome in Italy: A database of 29 STR markers 2011 Presciuttini S; Toni C; Alù M; Asmundo A; Baldassarri L; Barbaro A; Caenazzo L; Carnevali E; Cerri N; D’Aloia E; Di Nunzio C; Onofri V; Peloso G; Pelotti S; Piccinini A; Robino C; Turrina S; Venturi M; Domenici R
X-Hinter 2011 A. Panisson; R. Schifanella; G. Ruffo
X-hinter: a framework for implementing social oriented recommender systems 2008 A. Panisson; G. Ruffo; R. Schifanella
X-Klaim and Klava: Programming Mobile Code 2002 Lorenzo Bettini;Rocco De Nicola;Rosario Pugliese
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene. 1996 RENIERI A ;BRUTTINI M ;GALLI L ;ZANELLI P ;NERI T ;ROSSETTI S ;TURCO A ;HEISKARI N ;ZHOU J ;GUSMANO R ;MASSELLA L ;BANFI G ;SCOLARI F ;SESSA A ;RIZZONI G ;TRYGGVASON K ;PIGNATTI PF ;SAVI M ;BALLABIO A ;DE MARCHI M
X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A "European Community Alport Syndrome Concerted Action" Study 2003 JAIS JP; KNEBELMANN B; GIATRAS I; M. DE MARCHI; RIZZONI GF; RENIERI A; WEBER M; GROSS O; NETZER KO; FLINTER F; PIRSON Y; DAHAN K; WIESLANDER J; PERSSON U; TRYGGVASON K; MARTIN P; HERTZ PM; SCHRDER C; SANAK M; CARVALHO MF; SAUS J; ANTIGNAC C; SMEETS H AND GUBLER MC
X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males. 2000 JAIS JP; KNEBELMANN B; GIATRAS I; DE MARCHI M; RIZZONI G; RENIERI A; WEBER M; GROSS O; NETZER KO; FLINTER F; PIRSON Y; VERELLEN C; WIESLANDER J; PERSSON U; TRYGGVASON K; MARTIN P; HERTZ JM; SCHRÖDER C; SANAK M; KREJCOVA S; CARVALHO MF; SAUS J; ANTIGNAC C; SMEETS H; GUBLER MC
X-linked Charcot-Marie-Tooth polyneuropathy due to mutation of the connexin-32 gene: revision of our cases of genetic neuropathies and identification of three affected families. 2003 Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L.
[X-linked congenital hydrocephalus. Description of a case] 1978 SPADA A ;DE MARCHI M ;MELLANO G
X-linked ectodermal dysplasia. Presentation of 2 cases. 1984 Landi M; Ricca V; Oggero R; Guardamagna O; Cortelazzo MV; Sandrucci M.
X-Linked Hereditary Nephropathy in Navasota Dogs: Clinical Pathology, Morphology, and Gene Expression During Disease Progression 2016 Benali S.L; Lees G.E.; Nabity M.B.; Aricò A.; Drigo M.; Gallo E.; Giantin M.; Aresu L.
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 2019 Emma F.; Cappa M.; Antoniazzi F.; Bianchi M.L.; Chiodini I.; Eller Vainicher C.; Di Iorgi N.; Maghnie M.; Cassio A.; Balsamo A.; Baronio F.; De Sanctis L.; Tessaris D.; Baroncelli G.I.; Mora S.; Brandi M.L.; Weber G.; D'Ausilio A.; Lanati E.P.
X-Linked Immunodeficient Mice With No Functional Bruton's Tyrosine Kinase Are Protected From Sepsis-Induced Multiple Organ Failure 2020 O'Riordan C.E.; Purvis G.S.D.; Collotta D.; Krieg N.; Wissuwa B.; Sheikh M.H.; Ferreira Alves G.; Mohammad S.; Callender L.A.; Coldewey S.M.; Collino M.; Greaves D.R.; Thiemermann C.
X-linked situs abnormalities result from mutations in ZIC3 1997 Gebbia M; Ferrero GB; Pilia G; Bassi MT; Aylsworth A; Penman-Splitt M; Bird LM; Bamforth JS; Burn J; Schlessinger D; Nelson DL; Casey B.
X-linked thrombocytopenia and Wiskott Aldrich syndrome are allelic diseases with mutations in the WASP gene 1995 VILLA A; NOTARANGELO L; MACCHI P; MANTUANO E; CAVAGNI G; BRUGNONI D; STRINA D; PATROSSO MC; U. RAMENGHI; SACCO MG; UGAZIO AG
X-Ray Absorption and Emission Spectroscopy for Catalysis 2016 Lamberti, Carlo; van Bokhoven, Jeroen A.
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