Expanding the phenotype associated to KMT2A variants: overlapping
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Descrição
DECIPHER: Supporting the interpretation and sharing of rare
The social phenotype associated with Wiedemann‐Steiner syndrome
Molecular and cellular issues of KMT2A variants involved in
PDF) Expanding the phenotype associated to KMT2A variants
Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new
Frontiers Novel variants and phenotypic heterogeneity in a
Missense variants causing Wiedemann-Steiner syndrome
Neurodevelopmental Disorders: From Genetics to Functional Pathways
About - DECIPHER v11.23
Expanding the neurodevelopmental phenotypes of individuals with de
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