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Expert Opinion on Medical Diagnostics
|
March 16, 2013
Molecular diagnostics for haemoglobinopathies
John Old, Shirley Henderson
Annals of Hematology
|
June 23, 2010
Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing
Anna Haywood, Helene Dreau, Adele Timbs, et al.
Plos One
|
July 25, 2014
IthaGenes: an interactive database for haemoglobin variations and epidemiology
Petros Kountouris, Carsten W Lederer, Pavlos Fanis, et al.
Hemoglobin
|
July 26, 2008
Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia
Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, et al.
Clinical Biochemistry
|
June 6, 2009
Incidence of haemoglobinopathies in various populations - the impact of immigration
Shirley Henderson, Adele Timbs, Janice McCarthy, et al.
Annals of Hematology
|
October 17, 2008
Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants
Kamran Moradkhani, Claude Préhu, John Old, et al.
Genetic Testing and Molecular Biomarkers
|
August 21, 2010
Neonatal screening for hemoglobinopathies: results of a public health system in South Brazil
Sandrine C Wagner, Simone M de Castro, Tatiana P Gonzalez, et al.
International Journal of Cancer
|
May 7, 2011
Colon cancer associated transcript-1: a novel RNA expressed in malignant and pre-malignant human tissues
Aviram Nissan, Alexander Stojadinovic, Stella Mitrani-Rosenbaum, et al.
Hemoglobin
|
August 7, 2009
An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project
Carsten W Lederer, A Nazli Basak, Yesim Aydinok, et al.
Nature Genetics
|
March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Belinda Giardine, Joseph Borg, Douglas R Higgs, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Expert Opinion on Medical Diagnostics
|
March 16, 2013
Molecular diagnostics for haemoglobinopathies
John Old, Shirley Henderson
Annals of Hematology
|
June 23, 2010
Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing
Anna Haywood, Helene Dreau, Adele Timbs, et al.
Plos One
|
July 25, 2014
IthaGenes: an interactive database for haemoglobin variations and epidemiology
Petros Kountouris, Carsten W Lederer, Pavlos Fanis, et al.
Hemoglobin
|
July 26, 2008
Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia
Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, et al.
Clinical Biochemistry
|
June 6, 2009
Incidence of haemoglobinopathies in various populations - the impact of immigration
Shirley Henderson, Adele Timbs, Janice McCarthy, et al.
Annals of Hematology
|
October 17, 2008
Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants
Kamran Moradkhani, Claude Préhu, John Old, et al.
Genetic Testing and Molecular Biomarkers
|
August 21, 2010
Neonatal screening for hemoglobinopathies: results of a public health system in South Brazil
Sandrine C Wagner, Simone M de Castro, Tatiana P Gonzalez, et al.
International Journal of Cancer
|
May 7, 2011
Colon cancer associated transcript-1: a novel RNA expressed in malignant and pre-malignant human tissues
Aviram Nissan, Alexander Stojadinovic, Stella Mitrani-Rosenbaum, et al.
Hemoglobin
|
August 7, 2009
An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project
Carsten W Lederer, A Nazli Basak, Yesim Aydinok, et al.
Nature Genetics
|
March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Belinda Giardine, Joseph Borg, Douglas R Higgs, et al.
Page
of 1