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Annals of Hematology|June 23, 2010
Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencingAnna Haywood, Helene Dreau, Adele Timbs, et al.
Hemoglobin|March 8, 2014
A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2Mohamed S M Khalil, Samy Marouf, David Element, et al.
Clinical Biochemistry|June 6, 2009
Incidence of haemoglobinopathies in various populations - the impact of immigrationShirley Henderson, Adele Timbs, Janice McCarthy, et al.
Blood Advances|January 4, 2018
Mutational analysis of disease relapse in patients allografted for acute myeloid leukemiaLynn Quek, Paul Ferguson, Marlen Metzner, et al.
Blood|August 24, 2012
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patternsAnna Schuh, Jennifer Becq, Sean Humphray, et al.
British Journal of Haematology|May 30, 2018
Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLLJenny Klintman, Katerina Barmpouti, Samantha J L Knight, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 28, 2018
The Light Chain IgLV3-21 Defines a New Poor Prognostic Subgroup in Chronic Lymphocytic Leukemia: Results of a Multicenter StudyBasile Stamatopoulos, Thomas Smith, Emerence Crompot, et al.
Blood|August 29, 2015
Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLLRomain Guièze, Pauline Robbe, Ruth Clifford, et al.
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