Expanding the phenotype associated to KMT2A variants: overlapping
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Expanding the genotypic and phenotypic spectrum in a diverse
Frontiers Novel variants and phenotypic heterogeneity in a
PDF) Clinical exome sequencing reveals locus heterogeneity and
Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an
Family A with KMT2A-associated Wiedemann-Steiner syndrome (WSS
Mutational spectrum and phenotypic variability of Duchenne
PDF] KMT2A: Umbrella Gene for Multiple Diseases
DECIPHER: Supporting the interpretation and sharing of rare
About - DECIPHER v11.23
Expanding the phenotype associated to KMT2A variants: overlapping
A. Location of reported KMT2A mutation: Electrophogram of egi 9 of
De Novo variants in the KMT2A (MLL) gene causing atypical
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por adulto (o preço varia de acordo com o tamanho do grupo)
