Journal article
Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations
Abstract
INTRODUCTION: Inherited bone marrow failure syndromes (IBMFSs) often have substantial phenotypic overlap, thus genotyping is often critical for establishing a diagnosis.
OBJECTIVES AND METHODS: To determine the genetic characteristics and mutation profiles of IBMFSs, a comprehensive population-based study that prospectively enrols all typical and atypical cases without bias is required. The Canadian Inherited Marrow Failure Study is such a …
Authors
Tsangaris E; Klaassen R; Fernandez CV; Yanofsky R; Shereck E; Champagne J; Silva M; Lipton JH; Brossard J; Michon B
Journal
Journal of Medical Genetics, Vol. 48, No. 9,
Publisher
BMJ
Publication Date
September 2011
DOI
10.1136/jmg.2011.089821
ISSN
0022-2593
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AllelesAnemia, AplasticAnemia, Diamond-BlackfanBone Marrow DiseasesBone Marrow Failure DisordersCohort StudiesExocrine Pancreatic InsufficiencyFanconi AnemiaFanconi Anemia Complementation Group A ProteinGenetic TestingHemoglobinuria, ParoxysmalHumansLipomatosisMutationProspective StudiesProteinsRibosomal ProteinsShwachman-Diamond Syndrome