Associated Papers
Molecular Diagnosis and Identification of Novel Pathogenic Variants in a Large Cohort of Italian Patients Affected by Polycystic Kidney Diseases.
Nigro E et al.
Genes, 2023
A Prospective Study of Genetic Variants in Infants with Congenital Unilateral Sensorineural Hearing Loss.
Johansson M et al.
Journal of Clinical Medicine, 2023
36675424 (PubMed )
Supplement: jcm-12-00495-s001.zip › Tables_S1_and_S2.pdf
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