Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis
对一名患有 22q11.2 缺失综合征和幼年特发性关节炎的个体进行基因组测序
期刊:Genes
影响因子:2.8
doi:10.3390/genes15040513
de Oliveira-Sobrinho, Ruy Pires; Appenzeller, Simone; Holanda, Ianne Pessoa; Heleno, Júlia Lôndero; Jorente, Josep; On Behalf Of The Rare Genomes Project Consortium; Vieira, Társis Paiva; Steiner, Carlos Eduardo
