Intellectual Disability in Patients with MODY Due to Hepatocyte Nuclear Factor 1B (HNF1B) Molecular Defects
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Renal and Extrarenal Phenotypes in Patients With Variants and Chromosome 17q12 Microdeletions.
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Genetic and Clinical Characterization of Patients with HNF1B-Related MODY in Croatia.
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Review of neurodevelopmental disorders in patients with HNF1B gene variations.
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Prenatal Diagnosis of Intragenic Variant-Associated Renal Disease by Exome Sequencing.
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