Rare heterozygous PCSK1 variants in human obesity : the contribution of the p.Y181H variant and a literature review
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Genes - ISSN 2073-4425-13:10 (2022) p. 1-10
Nonmosaic isodicentric Y chromosome : a rare cause of Azoospermia: from genetics to clinical practice
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Case reports in endocrinology - ISSN 2090-6501-2020 (2020) p. 1-5
Association of hereditary angioedema type 1 with developmental anomalies due to a large and unusual de novo pericentromeric rearrangement of chromosome 11 spanning the entire C1 inhibitor gene (SERPING1)
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The journal of allergy and clinical immunology. In practice - ISSN 2213-2198-7:4 (2019) p. 1352-+
Evaluation of a role for NPY and NPY2R in the pathogenesis of obesity by mutation and copy number variation analysis in obese children and adolescents
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Annals of human genetics - ISSN 0003-4800-82:1 (2018) p. 1-10
Study of copy number and DNA sequence variations in candidate genes for obesity
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Antwerpen, Universiteit Antwerpen, Faculteit Farmaceutische, Biomedische en Diergeneeskundige Wetenschappen, 2017,186 p.