Expanding the phenotype associated to KMT2A variants: overlapping
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Expanding the genotypic and phenotypic spectrum in a diverse
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Molecular and cellular issues of KMT2A variants involved in
Childhood-onset dystonia-causing KMT2B variants result in a
PDF] KMT2A: Umbrella Gene for Multiple Diseases
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Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an
Molecular and cellular issues of KMT2A variants involved in
A. Location of reported KMT2A mutation: Electrophogram of egi 9 of
PDF] KMT2A: Umbrella Gene for Multiple Diseases
PDF] KMT2A: Umbrella Gene for Multiple Diseases
Childhood-onset dystonia-causing KMT2B variants result in a
Neurodevelopmental Disorders: From Genetics to Functional Pathways
PDF) Clinical exome sequencing reveals locus heterogeneity and