Associated Papers
CUX1 variant and 9p deletion: expanding the spectrum and resolving variable GDD/ID in a family.
Liu H et al.
Bmc Medical Genomics, 2025
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.
Oppermann H et al.
European Journal of Human Genetics : Ejhg, 2023
Acquired somatic variants in inherited myeloid malignancies.
Armes H et al.
Leukemia, 2022
35140362 (PubMed )
Supplement: 41375_2022_1515_MOESM3_ESM.xlsx › Somatic_variants
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