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Plos One|September 2, 2016
Diversity of the Genes Implicated in Algerian Patients Affected by Usher SyndromeSamia Abdi, Amel Bahloul, Asma Behlouli, et al.Plos One|March 24, 2015
Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patientsZied Riahi, Crystel Bonnet, Rim Zainine, et al.Orphanet Journal of Rare Diseases|June 15, 2014
Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?Laurent Enaud, Alice Hadchouel, Aurore Coulomb, et al.Plos One|June 14, 2014
Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafnessZied Riahi, Crystel Bonnet, Rim Zainine, et al.Respiratory Medicine|July 23, 2017
Heterogeneity of lung disease associated with NK2 homeobox 1 mutationsElodie Nattes, Stephanie Lejeune, Ania Carsin, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2012
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 geneDomitille Gras, Laurence Jonard, Emmanuel Roze, et al.Journal of Medical Genetics|November 1, 2022
New insights into CC2D2A-related Joubert syndromeMadeleine Harion, Leila Qebibo, Audrey Riquet, et al.Pageof 2