Associated Papers
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+).
Rivera-Munoz EA et al.
European Journal of Human Genetics : Ejhg, 2025
40913078 (PubMed )
Supplement: NIHMS2114636-supplement-Supplemental_Table_S1.xlsx › Table_S1
MED13L-related disorder characterized by severe motor speech impairment.
Mitchel MW et al.
Journal of Neurodevelopmental Disorders, 2025
MED13L-related disorder characterized by severe motor speech impairment.
Mitchel MW et al.
Research Square, 2024
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