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Bailliere'S Best Practice & Research. Clinical Haematology|August 5, 2000
Glucose-6-phosphate dehydrogenase deficiencyA Mehta, P J Mason, T J VulliamyBlood|October 6, 1997
Skewed X-inactivation in carriers of X-linked dyskeratosis congenitaT J Vulliamy, S W Knight, I Dokal, et al.Blood Cells, Molecules & Diseases|March 22, 2001
Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenitaT J Vulliamy, S W Knight, P J Mason, et al.Human Heredity|May 1, 1996
Molecular characterization of G6PD deficiency in OmanS Daar, T J Vulliamy, J Kaeda, et al.European Journal of Biochemistry|December 1, 1988
The production of normal and variant human glucose-6-phosphate dehydrogenase in cos cellsP J Mason, T J Vulliamy, N S Foulkes, et al.Human Genetics|May 31, 2001
Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosisS W Knight, T J Vulliamy, B Morgan, et al.Blood Cells, Molecules & Diseases|June 1, 1999
Human hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) encoded at 1p36: coding sequence and expressionP J Mason, D Stevens, A Diez, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1991
Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-T J Vulliamy, A Othman, M Town, et al.Human Genetics|March 1, 1992
Molecular heterogeneity underlying the G6PD Mediterranean phenotypeC M Corcoran, V Calabrò, G Tamagnini, et al.Blood|August 10, 1999
Dyskeratosis congenita caused by a 3' deletion: germline and somatic mosaicism in a female carrierT J Vulliamy, S W Knight, N S Heiss, et al.Pageof 190