Associated Papers
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.
Bekheirnia MR et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
Prospective investigation of FOXP1 syndrome.
Siper PM et al.
Molecular Autism, 2017
29090079 (PubMed )
Supplement: 13229_2017_172_MOESM2_ESM.xlsx › Supplementary_Table_2
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