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Biochimie|September 11, 2007
Dyskeratosis congenita: the diverse clinical presentation of mutations in the telomerase complexT J Vulliamy, I DokalBailliere'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.Human Genetics|April 1, 1993
G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish JewsA Oppenheim, C L Jury, D Rund, et al.Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1991
Linkage disequilibrium of polymorphic sites in the G6PD gene in African populations and the origin of G6PD A-T J Vulliamy, A Othman, M Town, et al.Genomics|February 1, 1997
Organization of the human protein 4.1 genomic locus: new insights into the tissue-specific alternative splicing of the pre-mRNAF Baklouti, S C Huang, T J Vulliamy, et al.Blood|September 1, 1995
Severe hemolytic anemia associated with the homozygous state for an unstable hemoglobin variant (Hb Bushwick)P Srivastava, J S Kaeda, D Roper, 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.Pageof 4