Associated Papers
MicroRNAs and the Diagnosis of Childhood Acute Lymphoblastic Leukemia: Systematic Review, Meta-Analysis and Re-Analysis with Novel Small RNA-Seq Tools.
Kyriakidis I et al.
Cancers, 2022
36010971 (PubMed )
Supplement: cancers-14-03976-s001.zip › Supplementary_Table_S1.pdf
Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia.
Gutierrez-Camino A et al.
Epigenomics, 2020
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Takata A et al.
Nature Communications, 2019
31175295 (PubMed )
Supplement: 41467_2019_10482_MOESM8_ESM.xlsx › Supplementary_Data_5
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › T2
Screening of Variations in CD22 Gene in Children with B-Precursor Acute Lymphoblastic Leukemia.
Aslar Oner D et al.
Genetic Testing and Molecular Biomarkers, 2016
Association of CD22 gene polymorphism with susceptibility to limited cutaneous systemic sclerosis.
Hitomi Y et al.
Tissue Antigens, 2007
Identification of the gene variations in human CD22.
Hatta Y et al.
Immunogenetics, 1999
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