Publications by authors named "Matthew Oakley"

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Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis.
Barnaby Clark, Claire Shooter, Frances Smith, David Brawand, Laura Steedman, Matthew Oakley

Br J Haematol· January 2018

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A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin.
Graham R Serjeant, Beryl E Serjeant, Ian R Hambleton, Matthew Oakley, Swee Lay Thein

Hemoglobin· May 2017

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First reported duplication of the entire beta globin gene cluster causing an unusual sickle cell trait phenotype.
Claire Shooter, Tania Senior McKenzie, Matthew Oakley, Tracey Jacques, Barnaby Clark

Br J Haematol· July 2015

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Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobin.
Sarmad Toma, María Tenorio, Matthew Oakley, Swee Lay Thein, Barnaby E Clark

Hemoglobin· September 2014

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A novel 506kb deletion causing εγδβ thalassemia.
Helen Rooks, Barnaby Clark, Steve Best, Peter Rushton, Matthew Oakley

Blood Cells Mol Dis· March 2013

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Repetitive posterior iliac crest autograft harvest resulting in an unstable pelvic fracture and infected non-union: case report and review of the literature.
Matthew J Oakley, Wade R Smith, Steven J Morgan, Navid M Ziran, Bruce H Ziran

Patient Saf Surg· December 2007

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Pediatric pelvic fractures.
Wade R Smith, Matthew Oakley, Steven J Morgan

J Pediatr Orthop· April 2004

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