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Trismus in the paediatric population.
Shires PM, Chow G. Shires PM, et al. Among authors: chow g. Dev Med Child Neurol. 2015 Apr;57(4):339-43. doi: 10.1111/dmcn.12636. Epub 2014 Nov 19. Dev Med Child Neurol. 2015. PMID: 25407568 Free article. Review.
The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.
Rodríguez Cruz PM, Cossins J, Estephan EP, Munell F, Selby K, Hirano M, Maroofin R, Mehrjardi MYV, Chow G, Carr A, Manzur A, Robb S, Munot P, Wei Liu W, Banka S, Fraser H, De Goede C, Zanoteli E, Conti Reed U, Sage A, Gratacos M, Macaya A, Dusl M, Senderek J, Töpf A, Hofer M, Knight R, Ramdas S, Jayawant S, Lochmüller H, Palace J, Beeson D. Rodríguez Cruz PM, et al. Among authors: chow g. Brain. 2019 Jun 1;142(6):1547-1560. doi: 10.1093/brain/awz107. Brain. 2019. PMID: 31081514 Free PMC article.
Solitary cervical osteochondroma in a 9-year-old child.
Zinna SS, Khan A, Chow G. Zinna SS, et al. Among authors: chow g. Pediatr Neurol. 2013 Sep;49(3):218-9. doi: 10.1016/j.pediatrneurol.2013.04.017. Epub 2013 Jul 5. Pediatr Neurol. 2013. PMID: 23835275 No abstract available.
Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain.
Logan CV, Cossins J, Rodríguez Cruz PM, Parry DA, Maxwell S, Martínez-Martínez P, Riepsaame J, Abdelhamed ZA, Lake AV, Moran M, Robb S, Chow G, Sewry C, Hopkins PM, Sheridan E, Jayawant S, Palace J, Johnson CA, Beeson D. Logan CV, et al. Among authors: chow g. Am J Hum Genet. 2015 Dec 3;97(6):878-85. doi: 10.1016/j.ajhg.2015.10.017. Epub 2015 Nov 25. Am J Hum Genet. 2015. PMID: 26626625 Free PMC article.
296 results