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Publications by Michael J. Allingham
Bilateral Proliferative Retinopathy Associated With Hoyeraal-Hreidarsson Syndrome, a Severe Form of Dyskeratosis Congenita
Ophthalmic Surgery Lasers and Imaging Retina
Medicine
Ophthalmology
Surgery
Related publications
Telomerase Reverse-Transcriptase Homozygous Mutations in Autosomal Recessive Dyskeratosis Congenita and Hoyeraal-Hreidarsson Syndrome
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
American Journal of Human Genetics
Genetics
A Recessive Founder Mutation in Regulator of Telomere Elongation Helicase 1, RTEL1, Underlies Severe Immunodeficiency and Features of Hoyeraal Hreidarsson Syndrome
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
A Vietnamese Case of Dyskeratosis Congenita
Our Dermatology Online
Dyskeratosis Congenita Caused by a Novel TERT Point Mutation in Siblings With Pancytopenia and Exudative Retinopathy
Pediatric Blood and Cancer
Oncology
Child Health
Hematology
Perinatology
Medicine
Pediatrics
Function of Apollo (SNM1B) at Telomere Highlighted by a Splice Variant Identified in a Patient With Hoyeraal-Hreidarsson Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Severe Proliferative Retinopathy in a Patient With Advanced Muscular Dystrophy
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Telomere Length Is Associated With Disease Severity and Declines With Age in Dyskeratosis Congenita
Haematologica
Hematology
Advances in the Understanding of Dyskeratosis Congenita
British Journal of Haematology
Hematology
