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Journal of Assisted Reproduction and Genetics|April 18, 2016
A new mutation identified in SPATA16 in two globozoospermic patientsElias ElInati, Camille Fossard, Ozlem Okutman, et al.
Journal of Pediatric Genetics|September 13, 2016
Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical TraitsHela Ben Khelifa, Molka Kammoun, Hanene Hannachi, et al.
International Journal of Fertility & Sterility|June 24, 2018
Subtelomeric Rearrangements in Patients with Recurrent MiscarriageAmani Hajlaoui, Wafa Slimani, Molka Kammoun, et al.
Expert Review of Medical Devices|November 28, 2019
Device profile of the heartware HVAD system as a bridge-to-transplantation in patients with advanced heart failure: overview of its safety and efficacySilvia Mariani, Jasmin Sarah Hanke, Tong Li, et al.
Journal of Pediatric Genetics|September 15, 2016
Cytogenetic analysis in a large series of children with non-syndromic mental retardationInesse Ben Abdallah Bouhjar, Abir Gmidène, Soumaya Mougou-Zrelli, et al.
Diagnostics (Basel, Switzerland)|June 27, 2024
Surgical Therapy of Infective Prosthesis Endocarditis following TAVI: A Single Center's ExperienceAlexander Weymann, Ali Saad Merzah, Arian Arjomandi Rad, et al.
Expert Review of Medical Devices|March 3, 2020
Minimally invasive left ventricular assist device implantation: optimizing device design for this approachAnamika Chatterjee, Silvia Mariani, Jasmin S Hanke, et al.
Journal of Pediatric Genetics|September 15, 2016
Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patientsInesse B Abdallah-Bouhjar, Soumaya Mougou-Zerelli, Hanene Hannachi, et al.
BMC Medical Genetics|February 8, 2020
Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotypeMeriam Hadj Amor, Sarra Dimassi, Amel Taj, et al.
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