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Mayo Clinic Proceedings, ISSN 0025-6196, 09/2019, Volume 94, Issue 9, pp. 1668 - 1669
Journal Article
Hematology/Oncology Clinics of North America, ISSN 0889-8588, 04/2009, Volume 23, Issue 2, pp. 215 - 231
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 04/2017, Volume 376, Issue 15, pp. 1460 - 1460
A 52-year-old man with a history of unexplained pancytopenia presented with cough and dyspnea. Findings on physical examination were suggestive of dyskeratosis... 
MEDICINE, GENERAL & INTERNAL | Telomere - ultrastructure | Dyskeratosis Congenita - diagnosis | Humans | Male | Nail Diseases | Leukoplakia | Blood Cell Count | Dyskeratosis | Dyspnea | Pulmonary fibrosis | Pancytopenia | Bone marrow | Respiration | Cough | Index Medicus | Abridged Index Medicus
Journal Article
FEBS Letters, ISSN 0014-5793, 09/2010, Volume 584, Issue 17, pp. 3831 - 3838
Dyskeratosis congenita (DC) was originally defined as a rare inherited bone marrow failure (BMF) syndrome associated with distinct mucocutaneous features.... 
Dyskeratosis congenita | Anticipation | Pulmonary fibrosis | Telomerase | Telomere | Aplastic anemia | AML | bone marrow failure | telomeric repeat binding factor 1 | telomeric repeat binding factor 2 | osteoporosis | protection of telomeres 1 | TRF2 | TRF1 | dyskeratosis congenita | HHS | acute myeloid leukemia | pulmonary fibrosis | POT1 | TRF1-interacting nuclear factor | BMF | Hoyeraal Hreidarrson syndrome | myelodysplastic syndrome | MDS | TIN2 | RNA | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | FUNCTIONAL-CHARACTERIZATION | TERMINAL TRANSFERASE | CELL BIOLOGY | BIOPHYSICS | CLINICAL PRESENTATION | HUMAN FIBROBLASTS | MUTATIONS | TELOMERASE REVERSE-TRANSCRIPTASE | APLASTIC-ANEMIA | PULMONARY-FIBROSIS | Cell Division - genetics | Telomere - ultrastructure | Humans | Middle Aged | Genetic Diseases, Inborn - genetics | Dyskeratosis Congenita - genetics | Telomere-Binding Proteins - genetics | Telomerase - genetics | Aging - physiology | Neoplasms - genetics | Bone Marrow - pathology | Genetic Diseases, Inborn - enzymology | Dyskeratosis Congenita - pathology | Adult | Telomerase - metabolism | Aged | Mutation | Infant, Newborn | Neoplasms - epidemiology | Telomere - genetics | Osteoporosis | Respiratory tract diseases | Anemia | Leukemia | Index Medicus | aplastic anemia | telomerase | anticipation | telomere
Journal Article
Dermatology Online Journal, ISSN 1087-2108, 2014, Volume 20, Issue 9
Dyskeratosis congenita is a rare disorder that often leads to early death owing to a variety of complications and associated disorders. Early diagnosis and... 
Exanthema - etiology | Dyskeratosis Congenita - diagnosis | Liver Cirrhosis - complications | Dental Caries - complications | Humans | Blepharitis - complications | Male | Dyskeratosis Congenita - genetics | Child | Nails, Malformed - complications | Index Medicus
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