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1. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

2. DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

3. Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene

4. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

5. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

7. Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

8. List of contributors

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