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Expanding the phenotype associated to KMT2A variants: overlapping

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Last updated 04 março 2025
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the phenotype associated to KMT2A variants: overlapping
Molecular and cellular issues of KMT2A variants involved in
Expanding the phenotype associated to KMT2A variants: overlapping
Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new
Expanding the phenotype associated to KMT2A variants: overlapping
Childhood Acute Lymphoblastic Leukemia Treatment (PDQ®) - PDQ
Expanding the phenotype associated to KMT2A variants: overlapping
IJMS, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping
American Journal of Medical Genetics Part A: Vol 182, No 11
Expanding the phenotype associated to KMT2A variants: overlapping
Genes, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping
Epigenetic changes in human model KMT2A leukemias highlight early
Expanding the phenotype associated to KMT2A variants: overlapping
Childhood-onset dystonia-causing KMT2B variants result in a
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the neurodevelopmental phenotypes of individuals with de
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the neurodevelopmental phenotypes of individuals with de
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