Associated Papers
Artificial intelligence (AI)-assisted exome reanalysis greatly aids in the identification of new positive cases and reduces analysis time in a clinical diagnostic laboratory.
O'Brien TD et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2022
Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms.
Trelles MP et al.
Molecular Autism, 2021
34588003 (PubMed )
Supplement: 13229_2021_469_MOESM1_ESM.pdf
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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