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Carvill GL, Mefford HC. Microdeletion syndromes. Curr Opin Genet Dev 23: 232-239, 2013.","DOI":"10.1016\/j.gde.2013.03.004"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Chaisson MJ, Wilson RK, Eichler EE. Genetic variation and the <i>de novo<\/i> assembly of human genomes. Nat Rev Genet 16: 627-640, 2015.","DOI":"10.1038\/nrg3933"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. George AM, Love DR, Hayes I, Tsang B. Recurrent transmission of a 17q12 microdeletion and a variable clinical spectrum. Mol Syndromol 2: 72-75, 2012.","DOI":"10.1159\/000335344"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Wu HX, Li L, Zhang H, et al. Accurate diagnosis and heterogeneity analysis of a 17q12 deletion syndrome family with adulthood diabetes onset and complex clinical phenotypes. Endocrine 73: 37-46, 2021.","DOI":"10.1007\/s12020-021-02682-5"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Laffargue F, Bourthoumieu S, Llanas B, et al. Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. Arch Dis Child 100: 259-264, 2015.","DOI":"10.1136\/archdischild-2014-306810"},{"key":"6","unstructured":"6. Mitchel MW, Moreno-De-Luca D, Myers SM, et al. 17q12 recurrent deletion syndrome. In: GeneReviews<sup>\u00ae<\/sup>. Adam MP, Ardinger HH, Pagon RA, et al., Eds. Seattle, WA, 1993."},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Chen H, Singh RR, Lu X, et al. Genome-wide copy number aberrations and <i>HER2<\/i> and <i>FGFR1<\/i> alterations in primary breast cancer by molecular inversion probe microarray. Oncotarget 8: 10845-10857, 2017.","DOI":"10.18632\/oncotarget.14802"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Rasmussen M, Vestergaard EM, Graakjaer J, et al. 17q12 deletion and duplication syndrome in Denmark - a clinical cohort of 38 patients and review of the literature. 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Adalat S, Woolf AS, Johnstone KA, et al. <i>HNF1B<\/i> mutations associate with hypomagnesemia and renal magnesium wasting. J Am Soc Nephrol 20: 1123-1131, 2009.","DOI":"10.1681\/ASN.2008060633"},{"key":"23","doi-asserted-by":"crossref","unstructured":"23. Stiles CE, Thuraisingham R, Bockenhauer D, Platts L, Kumar AV, Korbonits M. <i>De novo<\/i> HNF1 homeobox B mutation as a cause for chronic, treatment-resistant hypomagnesaemia. Endocrinol Diabetes Metab Case Rep 2018: 17-0120, 2018.","DOI":"10.1530\/EDM-17-0120"},{"key":"24","doi-asserted-by":"crossref","unstructured":"24. Li HJ, Groden C, Hoenig MP, et al. Case report: extreme coronary calcifications and hypomagnesemia in a patient with a 17q12 deletion involving <i>HNF1B<\/i>. BMC Nephrol 20: 353, 2019.","DOI":"10.1186\/s12882-019-1533-5"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25. Hardcastle AJ, Liskova P, Bykhovskaya Y, et al. 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