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For: Xiao TL, Zhang J, Liu L, Zhang B. Hepatocyte nuclear factor 1B mutation in a Chinese family with renal cysts and diabetes syndrome: A case report. World J Clin Cases 2021; 9(28): 8461-8469 [PMID: 34754854 DOI: 10.12998/wjcc.v9.i28.8461]
URL: https://www.wjgnet.com/2307-8960/full/v9/i28/8461.htm
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Yaroslav V. Dvoryanchikov, Rita I. Khusainova, Ildar R. Minniakhmetov, Ramil R. Salakhov, Kirill V. Smirnov, Saida A. Ibragimova, Ivan I. Golodnikov, Elena A. Sechko, Ekaterina A. Dobreva, Natalia G. Mokrysheva. A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization. Frontiers in Endocrinology 2026; 17 doi: 10.3389/fendo.2026.1819047
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