Associated Papers
Putative multiple myeloma susceptibility genes identified by exome sequencing of 347 familial and early-onset cases.
Pertesi M et al.
Leukemia, 2026
41254116 (PubMed )
Supplement: 41375_2025_2802_MOESM2_ESM.pdf
Clinical and genetic findings in autism spectrum disorders analyzed using exome sequencing.
Blázquez A et al.
Frontiers in Psychiatry, 2025
De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy.
Singh S et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2020
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