Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes
Por um escritor misterioso
Descrição
PDF] KMT2A: Umbrella Gene for Multiple Diseases
IJMS, Free Full-Text
Frontiers Sleep disturbances correlate with behavioral problems among individuals with Wiedemann-Steiner syndrome
Wiedemann-Steiner Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Frontiers Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome
Genes, Free Full-Text
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes
Genes, Free Full-Text
Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes
PDF] KMT2A: Umbrella Gene for Multiple Diseases
Children, Free Full-Text
De novo mutations in MLL cause Wiedemann-Steiner syndrome. - Abstract - Europe PMC
IJMS, Free Full-Text
Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome. - Abstract - Europe PMC
de
por adulto (o preço varia de acordo com o tamanho do grupo)