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Expanding the phenotype associated to KMT2A variants: overlapping

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Expanding the phenotype associated to KMT2A variants: overlapping
PDF] KMT2A: Umbrella Gene for Multiple Diseases
Expanding the phenotype associated to KMT2A variants: overlapping
Genes, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping
PDF) De Novo variants in the KMT2A (MLL) gene causing atypical
Expanding the phenotype associated to KMT2A variants: overlapping
IJMS, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping
American Journal of Medical Genetics Part A: Vol 182, No 11
Expanding the phenotype associated to KMT2A variants: overlapping
KMT2A rearranged acute lymphoblastic leukaemia: Unravelling the
Expanding the phenotype associated to KMT2A variants: overlapping
IJMS, Free Full-Text
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
Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new
Expanding the phenotype associated to KMT2A variants: overlapping
Genes, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping
PDF) Expanding the phenotype associated to KMT2A variants
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 genotypic and phenotypic spectrum in a diverse
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