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Journal of Pediatric Orthopedics|August 9, 2019
Osteofibrous Dysplasia of the Tibia in Children: Outcome Without ResectionDaniel Westacott, Peter Kannu, Jennifer Stimec, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Medial temporal lobe dysgenesis in hypochondroplasiaPeter Kannu, Ian M Hayes, Simone Mandelstam, et al.
Pediatric Dermatology|June 30, 2020
A novel ENPP1 mutation identified in a multigenerational family affected by Cole diseaseNiña Gabaton, Peter Kannu, Elena Pope, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 17, 2016
β-Catenin modulation in neurofibromatosis type 1 bone repair: therapeutic implicationsSaber Ghadakzadeh, Peter Kannu, Heather Whetstone, et al.
Stem Cells Translational Medicine|December 30, 2023
Direct Reprogramming of Fibroblasts to Osteoblasts: Techniques and MethodologiesAsghar Fallah, Alexander Beke, Connor Oborn, et al.
Sultan Qaboos University Medical Journal|July 18, 2013
Clinical Outcomes and Counselling Issues regarding Partial Trisomy of Terminal Xp in a Child with Developmental DelayKaren L Sheath, Roberto L Mazzaschi, Salim Aftimos, et al.
American Journal of Medical Genetics. Part A|March 15, 2006
Rapp-Hodgkin ectodermal dysplasia syndrome: the clinical and molecular overlap with Hay-Wells syndromePeter Kannu, Ravi Savarirayan, Linda Ozoemena, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotypeGregory Costain, Andrea Shugar, Pradeep Krishnan, et al.
Hormone Research in Paediatrics|June 13, 2017
PLS3 Mutations in X-Linked Osteoporosis: Clinical and Bone Characteristics of Two Novel MutationsPeter Kannu, Areej Mahjoub, Riyana Babul-Hirji, et al.
Genes|October 27, 2022
Exome Sequencing Identifies a Biallelic GALNS Variant (p.Asp233Asn) Causing Mucopolysaccharidosis Type IVA in a Pakistani Consanguineous FamilySaima Ghafoor, Karina da Costa Silveira, Raheel Qamar, et al.
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