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Matthew Oakley

Showing results (1-10 of 6) with videos related to

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Journal of Pediatric Orthopedics|December 17, 2003
Pediatric pelvic fracturesWade R Smith, Matthew Oakley, Steven J Morgan
Hemoglobin|October 23, 2013
Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobinSarmad Toma, María Tenorio, Matthew Oakley, et al.
British Journal of Haematology|December 19, 2014
First reported duplication of the entire beta globin gene cluster causing an unusual sickle cell trait phenotypeClaire Shooter, Tania Senior McKenzie, Matthew Oakley, et al.
Hemoglobin|September 6, 2017
A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal HemoglobinGraham R Serjeant, Beryl E Serjeant, Ian R Hambleton, et al.
Blood Cells, Molecules & Diseases|June 9, 2012
A novel 506kb deletion causing εγδβ thalassemiaHelen Rooks, Barnaby Clark, Steve Best, et al.
British Journal of Haematology|July 30, 2016
Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysisBarnaby Clark, Claire Shooter, Frances Smith, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of Pediatric Orthopedics|December 17, 2003
Pediatric pelvic fracturesWade R Smith, Matthew Oakley, Steven J Morgan
Hemoglobin|October 23, 2013
Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobinSarmad Toma, María Tenorio, Matthew Oakley, et al.
British Journal of Haematology|December 19, 2014
First reported duplication of the entire beta globin gene cluster causing an unusual sickle cell trait phenotypeClaire Shooter, Tania Senior McKenzie, Matthew Oakley, et al.
Hemoglobin|September 6, 2017
A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal HemoglobinGraham R Serjeant, Beryl E Serjeant, Ian R Hambleton, et al.
Blood Cells, Molecules & Diseases|June 9, 2012
A novel 506kb deletion causing εγδβ thalassemiaHelen Rooks, Barnaby Clark, Steve Best, et al.
British Journal of Haematology|July 30, 2016
Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysisBarnaby Clark, Claire Shooter, Frances Smith, et al.
Pageof 1