A. Gallienne

发表

Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations

S. Henderson, A. Timbs, D. Dziedzic, 2016, Hemoglobin.

Prenatal Diagnosis of Hemoglobinopathies by Pyrosequencing: A More Sensitive and Rapid Approach to Fetal Genotyping

S. Henderson, A. Timbs, J. Old, 2012, Hemoglobin.

Incidence of haemoglobinopathies in various populations - the impact of immigration.

A. Schuh, S. Henderson, A. Timbs, 2009, Clinical biochemistry.

Genetic basis of hereditary persistence of fetal haemoglobin

A. Gallienne, 2013 .

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′2

A. Schuh, S. Henderson, A. Timbs, 2014, Hemoglobin.

Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults

A. Schuh, S. Henderson, J. Old, 2012, Haematologica.

Characterization of Hb Lepore Variants in the UK Population

S. Henderson, J. Old, A. Gallienne, 2015, Hemoglobin.

A combination of two novel alpha globin variants Hb Bridlington (HBA1) and Hb Taybe (HBA2) resulting in severe hemolysis, pulmonary hypertension, and death

S. Henderson, Q. Hill, A. Gallienne, 2015, Hematology.

Characterization of a Novel Deletion Causing β-Thalassemia Major in an Afghan Family

A. Schuh, S. Henderson, P. Bignell, 2010, Hemoglobin.

Multiplex Ligation-Dependent Probe Amplification Identification of 17 Different β-Globin Gene Deletions (Including Four Novel Mutations) in the Uk Population

A. Schuh, S. Henderson, A. Timbs, 2009, Hemoglobin.

Incidence of haemoglobinopathies in various populations - the impact of immigration.

A. Schuh, S. Henderson, A. Timbs, 2009, Clinical biochemistry.