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Mostrati risultati da 298.222 a 298.241 di 299.245
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis 2021 Atsushi, Tanaka,Group, Italian PBC Genetics Study + GASTROENTEROLOGY - -
X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis 2021 Cazzagon N.Fabris L. + GASTROENTEROLOGY - -
X FIERA DI MILANO CAMPIONARIA INTERNAZIONALE, Milano, 12-28 aprile 1929 2017 Manfren, Priscilla - - Esporre l'Italia coloniale. Interpretazioni dell'alterità
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms. 1994 MOSTACCIUOLO, MARIA LUISA + JOURNAL OF MEDICAL GENETICS - -
La X Regio 1990 PROSDOCIMI, ALDO + - - Cultura popolare del Veneto. L'ambiente e il paesaggio
X(5) critical-point symmetries in138Gd 2012 VITTURI, ANDREAFORTUNATO, LORENZO + JOURNAL OF PHYSICS. CONFERENCE SERIES - -
X--ray Filaments from Cosmological Simulations 2001 PANTANO, ORNELLA + - - Science and Supercomputing at CINECA - 2001 Report
X-bracket. A high-ductility and dissipative connection for earthquake-resistant cross-laminated timber structures 2019 Scotta, RobertoMarchi, LucaTrutalli, DavidePozza, Luca - - -
X-bracket. A high-ductility and dissipative connection for earthquake-resistant cross-laminated timber structures 2019 Scotta RobertoMarchi LucaTrutalli Davide + - - -
X-chromosome in Italy: A database of 29 STR markers 2011 CAENAZZO, LUCIANA + FORENSIC SCIENCE INTERNATIONAL: GENETICS - FORENSIC SCIENCE INTERNATIONAL: GENETICS
X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patients 2003 PEGORARO, ELENAVETTORI, ANDREAMOSTACCIUOLO, MARIA LUISA + AMERICAN JOURNAL OF MEDICAL GENETICS. PART A - -
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant. 1996 PEGORARO, ELENAZeviani MANGELINI, CORRADO + AMERICAN JOURNAL OF MEDICAL GENETICS - -
X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy 2007 Zeviani, Massimo + MOLECULAR VISION - -
X-linked brachytelephalangic chondrodysplasia punctata: a simple trait that is not so simple. 2009 Doimo MTREVISSON, EVACARRARO, SILVIACLEMENTI, MAURIZIOBARALDI, EUGENIOSALVIATI, LEONARDO + AMERICAN JOURNAL OF MEDICAL GENETICS. PART A - -
X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region. 1991 MOSTACCIUOLO, MARIA LUISA + HUMAN GENETICS - -
X-linked cutaneous mosaicism in a dog 2019 Ferro S.MEZZALIRA, GIORGIA + VETERINARY DERMATOLOGY - -
X-Linked Hereditary Nephropathy in Navasota Dogs: Clinical Pathology, Morphology, and Gene Expression During Disease Progression 2016 BENALI, SILVIA LUCIAARICO', ARIANNADRIGO, MICHELEGALLO, ENRICOGIANTIN, MERYARESU, LUCA + VETERINARY PATHOLOGY - -
X-linked thrombophilia with a mutant factor IX (factor IX Padua). 2009 SIMIONI, PAOLOTORMENE, DANIELAGAVASSO, SABRINABULATO, CRISTIANASPIEZIA, LUCARADU, CLAUDIA-MARIA + NEW ENGLAND JOURNAL OF MEDICINE - -
X-RAY STRUCTURE OF 4-ACETYL-5-METHYL-2-PHENYLIMIDAZOLE FORMED FROM 3-HYDROXYIMINOPENTANE-2,4-DIONE AND BENZYLAMINE" J. C. S. CHEM. COMM. (1977) 443-444 1977 ZANOTTI, GIUSEPPE + JOURNAL OF THE CHEMICAL SOCIETY, CHEMICAL COMMUNICATIONS - -
X-ray absorption analysis of the active site of Streptomyces antibioticus Tyrosinase upon binding of transition state analogue inhibitors 2007 BUBACCO, LUIGI + ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS - -
Mostrati risultati da 298.222 a 298.241 di 299.245
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