Expanding the phenotype associated to KMT2A variants: overlapping

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Expanding the phenotype associated to KMT2A variants: overlapping
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Expanding the phenotype associated to KMT2A variants: overlapping
Comparison of methylation episignatures in KMT2B- and KMT2D
Expanding the phenotype associated to KMT2A variants: overlapping
Resolution of Disease Phenotypes Resulting from Multilocus Genomic
Expanding the phenotype associated to KMT2A variants: overlapping
Frontiers Genetic Mosaicism in a Group of Patients With Cornelia
Expanding the phenotype associated to KMT2A variants: overlapping
Frontiers Phenotypic and Genetic Complexity in Pediatric
Expanding the phenotype associated to KMT2A variants: overlapping
Analysis of KMT2A mutations in Wiedemann-Steiner syndrome vs ID/DD
Expanding the phenotype associated to KMT2A variants: overlapping
Frontiers Epigenetic disorders: Lessons from the animals–animal
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the phenotype associated to KMT2A variants: overlapping
Expanding the phenotype associated to KMT2A variants: overlapping
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