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Case Reports in Genetics|October 18, 2012
Amino-Terminal Microdeletion within the CNTNAP2 Gene Associated with Variable Expressivity of Speech DelayAmel Al-Murrani, Fern Ashton, Salim Aftimos, et al.Journal of Genetic Counseling|October 18, 2016
Parents' Understanding of Genetics and HeritabilityBrittany Harding, Rylan Egan, Peter Kannu, et al.Journal of the American Academy of Dermatology|March 26, 2019
Unraveling incontinentia pigmenti: A comparison of phenotype and genotype variantsRebecca Wang, Irene Lara-Corrales, Peter Kannu, et al.Pediatric Rheumatology Online Journal|July 15, 2021
Lost bones: differential diagnosis of acro-osteolysis seen by the pediatric rheumatologistElizaveta Limenis, Jennifer Stimec, Peter Kannu, et al.Experimental Eye Research|December 18, 2024
Genetic variants in PIKFYVE: A review of ocular phenotypesEhsan Misaghi, Peter Kannu, Ian M MacDonald, et al.Bone Reports|August 1, 2025
Multigenerational genetic inheritance and clinical characteristics of the rare disease hypophosphatasia in 6 families: A case seriesPeter Kannu, Aliya A Khan, Mira Francis, et al.Clinical Dysmorphology|April 5, 2008
Characterizing the oculoauriculofrontonasal syndromeMichael T Gabbett, Stephen P Robertson, Roland Broadbent, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 25, 2023
Spondyloepimetaphyseal dysplasia with joint laxity type 2: Aggregating the literature and reporting on the life of a 66-year-old manAlexander Beke, Karina da Costa Silveira, Taryn Athey, et al.Bone Reports|September 22, 2025
Corrigendum to "Multigenerational genetic inheritance and clinical characteristics of the rare disease hypophosphatasia in 6 families: A case series" [Bone Rep. 26 (2025) 1-6 (101857)]Peter Kannu, Aliya A Khan, Mira Francis, et al.Journal of Pediatric Orthopedics|August 9, 2019
Osteofibrous Dysplasia of the Tibia in Children: Outcome Without ResectionDaniel Westacott, Peter Kannu, Jennifer Stimec, et al.Pageof 13