Expanding the phenotype associated to KMT2A variants: overlapping

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Expanding the phenotype associated to KMT2A variants: overlapping
PDF] KMT2A: Umbrella Gene for Multiple Diseases
Expanding the phenotype associated to KMT2A variants: overlapping
Integrated gene analyses of de novo variants from 46,612 trios
Expanding the phenotype associated to KMT2A variants: overlapping
Delineating the molecular and phenotypic spectrum of the SETD1B
Expanding the phenotype associated to KMT2A variants: overlapping
DECIPHER: Supporting the interpretation and sharing of rare
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
Genes, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping
PDF) De Novo variants in the KMT2A (MLL) gene causing atypical
Expanding the phenotype associated to KMT2A variants: overlapping
PDF) Clinical exome sequencing reveals locus heterogeneity and
Expanding the phenotype associated to KMT2A variants: overlapping
PDF) Expanding the phenotype associated to KMT2A variants
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the neurodevelopmental phenotypes of individuals with de
Expanding the phenotype associated to KMT2A variants: overlapping
Frontiers Novel variants and phenotypic heterogeneity in a
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the genotypic and phenotypic spectrum in a diverse
Expanding the phenotype associated to KMT2A variants: overlapping
PDF] KMT2A: Umbrella Gene for Multiple Diseases
de por adulto (o preço varia de acordo com o tamanho do grupo)