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Bosma arhinia microphthalmia syndrome: Clinical report and review of the literature - Brasseur - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
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SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain | Journal of Medical Genetics
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Alex Magee's research works | Belfast Health and Social Care Trust, Belfast (BHSCT) and other places
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Facioscapulohumeral Muscular Dystrophy 2, Digenic disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
