Expanding the phenotype associated to KMT2A variants: overlapping
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Descrição
Molecular and cellular issues of KMT2A variants involved in
Childhood-onset dystonia-causing KMT2B variants result in a
A de novo mutation of ADAMTS8 in a patient with Wiedemann–Steiner
Molecular and cellular issues of KMT2A variants involved in
Neurodevelopmental Disorders: From Genetics to Functional Pathways
Childhood-onset dystonia-causing KMT2B variants result in a
Mutually suppressive roles of KMT2A and KDM5C in behaviour
PDF) Expanding the phenotype associated to KMT2A variants
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