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Nature Communications, ISSN 2041-1723, 01/2014, Volume 5, Issue 1, pp. 5360 - 5360
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 04/2018, Volume 38, Issue 3, pp. 273 - 277
Journal Article
Pädiatrie & Pädologie, ISSN 0030-9338, 9/2015, Volume 50, Issue S2, pp. 98 - 102
Spezialisierte Zentren für seltene Erkrankungen müssen in besonderer Weise die interdisziplinäre Zusammenarbeit zwischen verschiedenen Fachgebieten in einem... 
Rare diseases | Pediatrics | Seltene Erkrankungen | Personalisierte Medizin | Medicine & Public Health | Academic medical centers | Hochdurchsatznukleotidsequenzierung | Personalized medicine | Humangenetik | Akademische medizinische Zentren | High-throughput nucleotide sequencing | Human genetics
Journal Article
Paediatrie und Paedologie, ISSN 0030-9338, 09/2015, Volume 50, Issue 2, p. 98
Spezialisierte Zentren fur seltene Erkrankungen mussen in besonderer Weise die interdisziplinare Zusammenarbeit zwischen verschiedenen Fachgebieten in einem... 
Medical colleges | Pharmacogenetics | Orphans | Health care industry | Genetics
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 11/2009, Volume 361, Issue 21, pp. 2033 - 2045
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2015, Volume 372, Issue 25, pp. 2409 - 2422
Journal Article
Gastroenterology, ISSN 0016-5085, 2012, Volume 143, Issue 2, pp. 347 - 355
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2007, Volume 39, Issue 1, pp. 86 - 92
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 136, Issue 4, pp. 993 - 1006.e1
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 01/2009, Volume 360, Issue 1, pp. 32 - 43
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 136, Issue 3, pp. 703 - 712.e10
Background The clinical and immunologic features of CD27 deficiency remain obscure because only a few patients have been identified to date. Objective We... 
Allergy and Immunology | CD27 deficiency | hemophagocytic lymphohistiocytosis | hypogammaglobulinemia | EBV-induced lymphoproliferation | Hodgkin lymphoma | NATURAL-KILLER-CELLS | READ ALIGNMENT | EBV INFECTION | SCID MICE | COMMON VARIABLE IMMUNODEFICIENCY | IMMUNOLOGY | NK CELLS | ALLERGY | LYMPHOPROLIFERATIVE DISORDER | CD27-CD70 INTERACTIONS | EPSTEIN-BARR-VIRUS | T-CELLS | Lymphohistiocytosis, Hemophagocytic - pathology | Hodgkin Disease - genetics | Hodgkin Disease - pathology | Humans | Child, Preschool | Infant | Male | Lymphoproliferative Disorders - immunology | Exome | Young Adult | Flow Cytometry | Epstein-Barr Virus Infections - genetics | Female | Lymphohistiocytosis, Hemophagocytic - genetics | Lymphohistiocytosis, Hemophagocytic - immunology | Tumor Necrosis Factor Receptor Superfamily, Member 7 - immunology | Uveitis - diagnosis | Epstein-Barr Virus Infections - immunology | Hodgkin Disease - diagnosis | Lymphohistiocytosis, Hemophagocytic - diagnosis | Immunophenotyping | Lymphoproliferative Disorders - genetics | Tumor Necrosis Factor Receptor Superfamily, Member 7 - genetics | Lymphoproliferative Disorders - pathology | Epstein-Barr Virus Infections - pathology | Homozygote | Lymphoproliferative Disorders - diagnosis | Uveitis - immunology | Adolescent | Epstein-Barr Virus Infections - diagnosis | Heterozygote | Hodgkin Disease - immunology | Tumor Necrosis Factor Receptor Superfamily, Member 7 - deficiency | Mutation | Uveitis - genetics | Uveitis - pathology | Genetic research | Medical colleges | Genetic aspects | Children | Health aspects | Immunodeficiency | Proteins | Human subjects | Antigens | Lymphocytes | Quality | Families & family life | Cytotoxicity | T cell receptors | Genomes | Kinases | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus
Journal Article