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Journal of Human Genetics|November 7, 2009
Is CFTR 621+3 A>G a cystic fibrosis causing mutation?Monica Forzan, Leonardo Salviati, Vanessa Pertegato, et al.
American Journal of Medical Genetics. Part A|October 20, 2009
X-linked brachytelephalangic chondrodysplasia punctata: a simple trait that is not so simpleAlberto Casarin, Francesca Rusalen, Mara Doimo, et al.
American Journal of Medical Genetics. Part A|March 7, 2013
Evaluation of tibial osteopathy occurrence in neurofibromatosis type 1 Italian patientsGuido Morcaldi, Maurizio Clementi, Giuliana Lama, et al.
Ophthalmology. Retina|May 4, 2019
Retinal Vascular and Neural Remodeling Secondary to Optic Nerve Axonal Degeneration: A Study Using OCT AngiographyRaffaele Parrozzani, Francesca Leonardi, Luisa Frizziero, et al.
Clinical Chemistry and Laboratory Medicine|March 18, 2015
Validation of CFTR intronic variants identified during cystic fibrosis population screening by a minigene splicing assayGianpietro Giorgi, Alberto Casarin, Eva Trevisson, et al.
Reproductive Toxicology (Elmsford, N.Y.)|April 18, 2013
Pregnancy outcome in women exposed to antiepileptic drugs: teratogenic role of maternal epilepsy and its pharmacologic treatmentMatteo Cassina, Arianna Dilaghi, Elena Di Gianantonio, et al.
Journal of Pediatric Surgery|April 3, 2019
Prevalence and survival of patients with anorectal malformations: A population-based studyMatteo Cassina, Francesco Fascetti Leon, Michele Ruol, et al.
Journal of Clinical and Experimental Neuropsychology|December 30, 2015
Clinical and genetic correlates of decision making in anorexia nervosaElena Tenconi, Daniela Degortes, Maurizio Clementi, et al.
The Journal of Headache and Pain|June 30, 2011
Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?Irene Toldo, Alice Bruson, Alberto Casarin, et al.
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