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Expanding the phenotype associated to KMT2A variants: overlapping

Por um escritor misterioso
Last updated 12 abril 2025
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the phenotype associated to KMT2A variants: overlapping
Frontiers Epigenetic disorders: Lessons from the animals–animal
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
The epileptology of Wiedemann-Steiner syndrome: Electroclinical
Expanding the phenotype associated to KMT2A variants: overlapping
Frontiers Novel variants and phenotypic heterogeneity 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
A de novo mutation of ADAMTS8 in a patient with Wiedemann–Steiner
Expanding the phenotype associated to KMT2A variants: overlapping
Neurodevelopmental Disorders: From Genetics to Functional Pathways
Expanding the phenotype associated to KMT2A variants: overlapping
Delineation of clinical features in Wiedemann – Steiner syndrome
Expanding the phenotype associated to KMT2A variants: overlapping
Genes, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping
Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the neurodevelopmental phenotypes of individuals with de
Expanding the phenotype associated to KMT2A variants: overlapping
IJMS, Free Full-Text
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