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Publications by R Arngrimsson

Dyskeratosis Congenita: Three Additional Families Show Linkage to a Locus in Xq28.

Journal of Medical Genetics

English

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A Vietnamese Case of Dyskeratosis Congenita

Our Dermatology Online

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Advances in the Understanding of Dyskeratosis Congenita

British Journal of Haematology

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Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita

American Journal of Human Genetics

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The Diagnosis and Treatment of Dyskeratosis Congenita: A Review

Journal of Blood Medicine

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Linkage of Autosomal Dominant Dystrophic Epidermolysis Bullosa in Three British Families to the Marker D3S2 Close to the COL7A1 Locus.

Journal of Medical Genetics

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Outcome of Haematopoietic Stem Cell Transplantation in Dyskeratosis Congenita

British Journal of Haematology

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Short Telomeres: From Dyskeratosis Congenita to Sporadic Aplastic Anemia and Malignancy

Translational Research

Occupational Health

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Clinical Utility Gene Card For: Dyskeratosis Congenita – Update 2015

European Journal of Human Genetics

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Dyskeratosis Congenita With a Novel Genetic Variant in the DKC1 Gene: A Case Report

BMC Medical Genetics

English