Expanding the phenotype associated to KMT2A variants: overlapping

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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
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
RXRA DT448/9PP generates a dominant active variant capable of
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
Digenic variant interpretation with hypothesis-driven explainable
Expanding the phenotype associated to KMT2A variants: overlapping
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Expanding the phenotype associated to KMT2A variants: overlapping
Transcriptome-based molecular subtypes and differentiation
Expanding the phenotype associated to KMT2A variants: overlapping
PDF] KMT2A: Umbrella Gene for Multiple Diseases
Expanding the phenotype associated to KMT2A variants: overlapping
Characterizing the molecular impact of KMT2D variants on the
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
About - DECIPHER v11.23
Expanding the phenotype associated to KMT2A variants: overlapping
Mutually suppressive roles of KMT2A and KDM5C in behaviour
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the phenotype associated to KMT2A variants: overlapping
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