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Diagnosis and clinical relevance of co-inheritance of haemoglobin D-Punjab/β+-thalassemia traits in an immigrant Afghan family
We report on a Pashtun family affected by haemoglobin D-Punjab/β+-thalassemia to increase the awareness of the increasing prevalence of haemoglobinopathies among primary care physicians. We highlight the diagnostic approach of these conditions and the benefits of genetic counselling.
Autores principales: | Huits, Ralph, Feyens, Anne-Marie, Lonneville, Niels, Peyrassol, Xavier, Adam, Anne-Sophie, Gulbis, Beatrice, Van Esbroeck, Marjan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685697/ https://www.ncbi.nlm.nih.gov/pubmed/35039448 http://dx.doi.org/10.1136/jclinpath-2021-208009 |
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