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Vernon Long

Showing results (11-20 of 15) with videos related to

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BMJ Open|March 23, 2017
Treatment trends for retinopathy of prematurity in the UK: active surveillance study of infants at riskGillian G W Adams, Catey Bunce, Wen Xing, et al.
Journal of Neurosurgery. Pediatrics|April 1, 2017
A proposal for a new classification of complications in craniosynostosis surgeryDmitri Shastin, Sharron Peacock, Velu Guruswamy, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|April 22, 2015
Monitoring the changing pattern of delivery of paediatric epilepsy surgery in England--an audit of a regional service and examination of national trendsDmitri Shastin, Suresh Chandrasekaran, Colin Ferrie, et al.
American Journal of Human Genetics|December 23, 2023
A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genesErica L Harris, Vincent Roy, Martin Montagne, et al.
Human Mutation|March 17, 2010
Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypesKatherine V Towns, Athina Kipioti, Vernon Long, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
BMJ Open|March 23, 2017
Treatment trends for retinopathy of prematurity in the UK: active surveillance study of infants at riskGillian G W Adams, Catey Bunce, Wen Xing, et al.
Journal of Neurosurgery. Pediatrics|April 1, 2017
A proposal for a new classification of complications in craniosynostosis surgeryDmitri Shastin, Sharron Peacock, Velu Guruswamy, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|April 22, 2015
Monitoring the changing pattern of delivery of paediatric epilepsy surgery in England--an audit of a regional service and examination of national trendsDmitri Shastin, Suresh Chandrasekaran, Colin Ferrie, et al.
American Journal of Human Genetics|December 23, 2023
A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genesErica L Harris, Vincent Roy, Martin Montagne, et al.
Human Mutation|March 17, 2010
Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypesKatherine V Towns, Athina Kipioti, Vernon Long, et al.
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