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1979, ISBN 9780702006982, 249
Book
1989, ISBN 9780702012815, Volume 2/no. 1., ix, 194
Book
1978, Volume 7 no.3., 232
Book
Current Opinion in Hematology, ISSN 1065-6251, 05/2008, Volume 15, Issue 3, pp. 162 - 168
Journal Article
1999, ISBN 0521641012, xii, 391
This book takes account of the most recent findings in laboratory research and clinical trials to provide a comprehensive and up-to-date reference on the... 
physiopathology | therapy | Anemia, Aplastic | Aplastic anemia
Book
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2017, Volume 23, Issue 9, pp. 1422 - 1428
Abstract Patients with inherited bone marrow failure syndromes (IBMFS) such as Fanconi anemia (FA), dyskeratosis congenita (DC), and Diamond Blackfan anemia... 
Hematology, Oncology and Palliative Medicine | Late effects | Dyskeratosis congenita | Pediatric allogeneic hematopoietic cell transplant | Fanconi anemia | Diamond Blackfan anemia | Inherited bone marrow failure syndromes | LONG-TERM SURVIVORS | Pediatric allogeneic | 4 DECADES | NATIONAL-CANCER-INSTITUTE | IMMUNOLOGY | CHRONIC HEALTH CONDITIONS | BIALLELIC MUTATIONS | FANCONI-ANEMIA | TRANSPLANTATION | hematopoietic cell transplant | INSTITUTE/PEDIATRIC BLOOD | DYSKERATOSIS-CONGENITA | DIAMOND-BLACKFAN ANEMIA | HEMATOLOGY | APLASTIC-ANEMIA | Bone Marrow Diseases - diagnosis | Humans | Anemia, Diamond-Blackfan - immunology | Hemoglobinuria, Paroxysmal - pathology | Anemia, Diamond-Blackfan - mortality | Dyskeratosis Congenita - mortality | Anemia, Aplastic - therapy | Fanconi Anemia - mortality | Transplantation, Homologous | Hemoglobinuria, Paroxysmal - immunology | Anemia, Aplastic - diagnosis | Bone Marrow Diseases - therapy | Dyskeratosis Congenita - diagnosis | Dyskeratosis Congenita - therapy | Anemia, Diamond-Blackfan - therapy | Hemoglobinuria, Paroxysmal - diagnosis | Child | Anemia, Aplastic - pathology | Hematopoietic Stem Cell Transplantation | International Cooperation | Bone Marrow Diseases - pathology | Consensus Development Conferences as Topic | Anemia, Diamond-Blackfan - diagnosis | Consensus | Fanconi Anemia - diagnosis | Bone Marrow Diseases - immunology | Survival Analysis | Fanconi Anemia - immunology | Fanconi Anemia - therapy | Hemoglobinuria, Paroxysmal - therapy | Dyskeratosis Congenita - immunology | Anemia, Aplastic - immunology | Pediatrics | Conferences, meetings and seminars | Immunodeficiency | Bone marrow | Genetic aspects | Transplantation | Medical screening | Conferences and conventions | Hematopoietic stem cells | Fanconi's anemia | Medical research | Epidemiology | Diseases | Medicine, Experimental | Children | dyskeratosis congenita | pediatric allogeneic hematopoietic cell transplant | late effects | inherited bone marrow failure syndromes
Journal Article
Clinical Chemistry, ISSN 0009-9147, 10/2017, Volume 63, Issue 10, pp. 1614 - 1623
BACKGROUND: There is much interest in the tissue of origin of circulating DNA in plasma. Data generated using DNA methylation markers have suggested that... 
ANEUPLOIDY | NONINVASIVE PRENATAL-DIAGNOSIS | BARR-VIRUS DNA | RAPID CLEARANCE | BLUEPRINT | EPIGENETIC SIGNATURE | CLASSIFICATION | FETAL DNA | MEDICAL LABORATORY TECHNOLOGY | CANCER | BLOOD | Erythropoiesis | beta-Thalassemia - pathology | Anemia - blood | Humans | Erythroblasts - metabolism | beta-Thalassemia - genetics | Anemia - pathology | Myelodysplastic Syndromes - blood | Anemia, Aplastic - blood | Anemia, Iron-Deficiency - blood | DNA - blood | Anemia, Aplastic - diagnosis | Anemia - genetics | DNA Methylation | Anemia, Aplastic - genetics | beta-Thalassemia - blood | Anemia, Aplastic - pathology | Diagnosis, Differential | Anemia - diagnosis | beta-Thalassemia - diagnosis | DNA - genetics | Myelodysplastic Syndromes - diagnosis | Anemia, Iron-Deficiency - diagnosis | Anemia, Iron-Deficiency - genetics | Anemia, Iron-Deficiency - pathology | Ferrochelatase - genetics | Myelodysplastic Syndromes - genetics | Myelodysplastic Syndromes - pathology | Erythroblasts - pathology | Genetic aspects | Diagnosis | Anemia | Erythrocytes | Iron | Blood | Blood plasma | Etiology | Lymphocytes | DNA methylation | Bone marrow | Differential diagnosis | Signatures | Deoxyribonucleic acid--DNA | Quantitative analysis | Nutrient deficiency | Ferrochelatase | Neutrophils | Aplastic anemia | Thalassemia | Patients | Loci | Hemopoiesis | Polymerase chain reaction | Erythroblasts | Epigenetics | Biomarkers | Methylation | Plasmas (physics)
Journal Article
British Journal of Haematology, ISSN 0007-1048, 05/2017, Volume 177, Issue 4, pp. 526 - 542
Summary The inherited bone marrow failure syndromes (IBMFS) typically present with significant cytopenias in at least one haematopoietic cell lineage that may... 
Fanconi anaemia | Shwachman Diamond syndrome | dyskeratosis congenita | Diamond Blackfan anaemia | inherited bone marrow failure | HOYERAAL-HREIDARSSON-SYNDROME | ACUTE MYELOGENOUS LEUKEMIA | SOMATIC MOSAICISM | FANCONI-ANEMIA | C-MPL MUTATIONS | CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA | CROSS-LINK REPAIR | DYSKERATOSIS-CONGENITA | DIAMOND-BLACKFAN ANEMIA | HEMATOLOGY | APLASTIC-ANEMIA | Exocrine Pancreatic Insufficiency - genetics | Bone Marrow Diseases - diagnosis | Humans | Exocrine Pancreatic Insufficiency - diagnosis | Dyskeratosis Congenita - genetics | Genetic Counseling | Neutropenia - congenital | Anemia, Aplastic - diagnosis | Neutropenia - diagnosis | Dyskeratosis Congenita - diagnosis | Fanconi Anemia - genetics | Genomics - methods | Hemoglobinuria, Paroxysmal - diagnosis | Neutropenia - genetics | Anemia, Aplastic - genetics | Telomere - genetics | Blood Platelet Disorders - genetics | Hemoglobinuria, Paroxysmal - genetics | Lipomatosis - genetics | Blood Platelet Disorders - diagnosis | Anemia, Diamond-Blackfan - diagnosis | Bone Marrow Diseases - genetics | Fanconi Anemia - diagnosis | Ribosomes - genetics | Anemia, Diamond-Blackfan - genetics | Lipomatosis - diagnosis | DNA Repair-Deficiency Disorders - genetics | Genetic research | Genomics | Fanconi's anemia | Dyskeratosis | Anemia | Diamonds | Disorders | Health risks | Cell lineage | Biology | Patients | Genetic screening | Gene sequencing | Pancytopenia | Bone marrow | Diagnostic systems | Genetic counselling | Cancer
Journal Article