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Publications by Tom Vulliamy

Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita

American Journal of Human Genetics
Genetics
2013English

Laboratory Diagnosis of G6PD Deficiency. A British Society for Haematology Guideline

British Journal of Haematology
Hematology
2020English

Clinical Utility Gene Card For: Dyskeratosis Congenita – Update 2015

European Journal of Human Genetics
Genetics
2014English

Isolation of Human Glucose-6-Phosphate Dehydrogenase (G6PD) cDNA Clones: Primary Structure of the Protein and Unusual 5′ Non-Coding Region

Nucleic Acids Research
Genetics
1986English

Telomerase Reverse-Transcriptase Homozygous Mutations in Autosomal Recessive Dyskeratosis Congenita and Hoyeraal-Hreidarsson Syndrome

Blood
BiochemistryImmunologyCell BiologyHematology
2007English

Targeted Disruption of Dkc1, the Gene Mutated in X-Linked Dyskeratosis Congenita, Causes Embryonic Lethality in Mice

Oncogene
Cancer ResearchGeneticsMolecular Biology
2002English

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