Expanding the phenotype associated to KMT2A variants: overlapping

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Expanding the phenotype associated to KMT2A variants: overlapping
Clonal hematopoiesis, somatic mosaicism, and age-associated
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
Expanding the neurodevelopmental phenotypes of individuals with de
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
Molecular and cellular issues of KMT2A variants involved in
Expanding the phenotype associated to KMT2A variants: overlapping
PDF) Clinical exome sequencing reveals locus heterogeneity and
Expanding the phenotype associated to KMT2A variants: overlapping
Evaluation of different variant classes in KMT2A in individuals
Expanding the phenotype associated to KMT2A variants: overlapping
RXRA DT448/9PP generates a dominant active variant capable of
Expanding the phenotype associated to KMT2A variants: overlapping
Genes, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping
PDF] KMT2A: Umbrella Gene for Multiple Diseases
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
Frontiers Novel variants and phenotypic heterogeneity in a
Expanding the phenotype associated to KMT2A variants: overlapping
PDF) Expanding the phenotype associated to KMT2A variants
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