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Human Mutation|September 20, 2006
The Italian XLMR bank: a clinical and molecular databaseC Pescucci, R Caselli, F Mari, et al.
The British Journal of Ophthalmology|September 4, 2010
Association between primary open-angle glaucoma (POAG) and WDR36 sequence variance in Italian families affected by POAGPaolo Frezzotti, Chiara Pescucci, Filomena Tiziana Papa, et al.
International Journal of Audiology|December 9, 2003
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian familiesFrancesca Di Leva, Adamo Pio D'Adamo, Luiaino Strollo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 16, 2010
EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndromeSabrina Buoni, Raffaella Zannolli, Claudio De Felice, et al.
Environmental Research|June 2, 2017
Nonlinear responses to waterborne cadmium exposure in zebrafish. An in vivo studyElisavet A Renieri, Dimitris G Sfakianakis, Athanasios A Alegakis, et al.
Clinical Journal of the American Society of Nephrology : CJASN|June 8, 2022
Digenic Alport SyndromeJudy Savige, Alessandra Renieri, Elisabet Ars, et al.
World Neurosurgery|May 11, 2019
Carotid Cavernous Fistulas and Dural Arteriovenous Fistulas of the Cavernous Sinus: Validation of a New Classification According to Venous DrainageGiuseppe Leone, Leonardo Renieri, Alejandro Enriquez-Marulanda, et al.
European Journal of Medical Genetics|May 22, 2007
A 2.6 Mb deletion of 6q24.3-25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic earsR Caselli, M A Mencarelli, F T Papa, et al.
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