Expanding the phenotype associated to KMT2A variants: overlapping
Descrição
American Journal of Medical Genetics Part A: Vol 182, No 11
Frontiers Phenotypic and Genetic Complexity in Pediatric
Expanding the neurodevelopmental phenotypes of individuals with de
Expanding the genotypic and phenotypic spectrum in a diverse
Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new
Expanding the neurodevelopmental phenotypes of individuals with de
Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new
Genes, Free Full-Text
The social phenotype associated with Wiedemann‐Steiner syndrome
About - DECIPHER v11.23
PDF] KMT2A: Umbrella Gene for Multiple Diseases
Childhood-onset dystonia-causing KMT2B variants result in a
de
por adulto (o preço varia de acordo com o tamanho do grupo)
