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机译:一种新颖的&粗体>&斜体> ptch1& /斜体>& /粗体>框架突变,导致Nevoid基础细胞癌综合征
Departments of Medical Genetics;
Departments of Division of EvolutionGenomic Science School of Biological Sciences Faculty of Biology MedicineHealth University of Manchester Manchester Academic Health Science Centre;
Departments of Division of EvolutionGenomic Science School of Biological Sciences Faculty of Biology MedicineHealth University of Manchester Manchester Academic Health Science Centre;
Departments of Dermatology Faculty of Medicine Ankara University Ankara Turkey;
Departments of Dermatology Faculty of Medicine Ankara University Ankara Turkey;
Departments of Medical Genetics;
Gorlin syndrome; Medulloblastoma; Nevoid basal cell carcinoma syndrome; PTCH1; SUFU;
机译:一种新颖的&粗体>&斜体> ptch1& /斜体>& /粗体>框架突变,导致Nevoid基础细胞癌综合征
机译:QTc高且
机译:HO综合征患者的皮肤显性表型:鉴定&智能> slc29a3& /斜体>基因的新突变
机译:PTCH1基因的新型突变激活了中国患有避免基底细胞癌综合征的中国家庭的Shh / Gli信号通路
机译:探索彩色视觉的神经机制:基于fMRI的大胆研究。
机译:日本家族尾样物基础细胞癌综合征的新型PTCH1突变
机译:一种新的PTCH1框架突变,导致Nevoid基础细胞癌综合征