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Orthodontics & Craniofacial Research|May 11, 2019
Examination of rare genetic variants in dental enamel genes: The potential role of next-generation sequencing in primary dental careEmily Farrow, Shankar Rengasamy Venugopalan, Isabelle Thiffault, et al.
American Journal of Medical Genetics. Part A|February 25, 2015
An infant with large fontanelles, aplasia cutis congenita, tessier facial cleft, polydactyly inversus, and toe syndactyly: a previously undescribed syndrome?Jessica Jackson, Paula Delk, Emily Farrow, et al.
Human Mutation|October 13, 2018
On the verge of diagnosis: Detection, reporting, and investigation of de novo variants in novel genes identified by clinical sequencingIsabelle Thiffault, Maxime Cadieux-Dion, Emily Farrow, et al.
Pediatrics|January 2, 2021
Rare Genetic Variants in Immune Genes and Neonatal Herpes Simplex Viral InfectionsLauren Cummings, Megan Tucker, Margaret Gibson, et al.
Indian Journal of Pediatrics|October 29, 2014
Molecular diagnosis of infantile Neuro axonal Dystrophy by Next Generation SequencingManisha Goyal, Sunita Bijarnia-Mahay, Stephen Kingsmore, et al.
Surgical Endoscopy|March 18, 2023
Can endoscopic follow-up after acute diverticulitis be rationalised?Harry Frederick Dean, Emily Britton, Emily Farrow, et al.
American Journal of Medical Genetics. Part A|September 10, 2016
Neonatal progeriod syndrome associated with biallelic truncating variants in POLR3AAllison M Jay, Robert L Conway, Isabelle Thiffault, et al.
Orthodontics & Craniofacial Research|May 11, 2019
A novel nonsense substitution identified in the AMIGO2 gene in an Occulo-Auriculo-Vertebral spectrum patientShankar Rengasamy Venugopalan, Emily Farrow, Pedro A Sanchez-Lara, et al.
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