Expanding the phenotype associated to KMT2A variants: overlapping
Por um escritor misterioso
Descrição
Frontiers Novel variants and phenotypic heterogeneity in a
RXRA DT448/9PP generates a dominant active variant capable of
Family A with KMT2A-associated Wiedemann-Steiner syndrome (WSS
Expanding the genotypic and phenotypic spectrum in a diverse
Molecular and cellular issues of KMT2A variants involved in
PDF] KMT2A: Umbrella Gene for Multiple Diseases
PDF) Clinical exome sequencing reveals locus heterogeneity and
Genes, Free Full-Text
Clonal hematopoiesis, somatic mosaicism, and age-associated
IJMS, Free Full-Text
Molecular and cellular issues of KMT2A variants involved in
Childhood-onset dystonia-causing KMT2B variants result in a
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por adulto (o preço varia de acordo com o tamanho do grupo)
