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- [24] Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndromeCLINICAL EPIGENETICS, 2020, 12 (01)Essinger, Carla论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, GermanyKarch, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Heidelberg Univ, Univ Childrens Hosp, Heidelberg, Germany Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, GermanyMoog, Ute论文数: 0 引用数: 0 h-index: 0机构: Heidelberg Univ, Inst Human Genet, Heidelberg, Germany Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, GermanyFekete, Gyorgy论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Dept Paediat 2, Budapest, Hungary Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, GermanyLengyel, Anna论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Dept Paediat 2, Budapest, Hungary Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, GermanyPinti, Eva论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Dept Paediat 2, Budapest, Hungary Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, GermanyEggermann, Thomas论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, GermanyBegemann, Matthias论文数: 0 引用数: 0 h-index: 0机构: Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, Germany Rhein Westfal TH Aachen, Inst Human Genet, Fac Med, Pauwelsstr 30, D-52074 Aachen, Germany
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