Showing results (171-180 of 621) with videos related to

Sort By:
Pageof 63
Archives of Dermatological Research|January 29, 2000
Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regionsM Fimiani, M Seri, P Rubegni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 18, 2021
A new mutation in DNM2 gene in a large Italian familyDiego Lopergolo, Silvia Bocci, Anna Maria Pinto, et al.
Gene|October 16, 2021
The ASIP gene in the llama (Lama glama): Alternative transcripts, expression and relation with color phenotypesM Anello, M S Daverio, S S Rodríguez, et al.
Genomics|September 24, 1999
KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologsM Piccini, F Vitelli, M Seri, et al.
Clinical Dysmorphology|October 18, 2016
Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetusesAnna Maria Pinto, Valentina Imperatore, Laura Bianciardi, et al.
Clinical and Experimental Rheumatology|August 1, 2019
Altered expression of RXFP1 receptor contributes to the inefficacy of relaxin-based anti-fibrotic treatments in systemic sclerosisClaudio Corallo, Anna Maria Pinto, Alessandra Renieri, et al.
Epilepsy Research|February 19, 2008
Epilepsy and electroencephalographic anomalies in chromosome 2 aberrations. A reviewSalvatore Grosso, Lucia Pucci, Paolo Curatolo, et al.
European Journal of Medical Genetics|February 9, 2019
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotypeAnnarita Giliberti, Aurora Currò, Filomena Tiziana Papa, et al.
Frontiers in Integrative Neuroscience|June 28, 2018
Functional Connectivity and Genetic Profile of a "Double-Cortex"-Like MalformationGiulia Sprugnoli, Giampaolo Vatti, Simone Rossi, et al.
International Journal of Molecular Sciences|March 2, 2016
Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory DistressValentina Imperatore, Maria Antonietta Mencarelli, Chiara Fallerini, et al.
Pageof 63