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机译:终端14Q32.33删除作为Agammaglobulinemia的新颖原因
Immunology Outpatient Clinic;
Immunology Outpatient Clinic;
Immunology Outpatient Clinic;
Department of Pediatrics Faculty of Medicine Comenius University and Children's University Hospital;
Department of Pediatrics Faculty of Medicine Comenius University and Children's University Hospital;
Immunology Outpatient Clinic;
Primary immunodeficiency; Agammaglobulinemia; B-cell defect; Microdeletion; 14q32.33;
机译:终端14Q32.33删除作为Agammaglobulinemia的新颖原因
机译:一个具有14q32.33染色体遗传0.31Mb微缺失的孩子:进一步确定14q32缺失综合征的关键区域
机译:阵列比较基因组杂交技术检测Dubowitz综合征患者的14q32.33染色体缺失
机译:苏云金芽孢杆菌Cry1Ie N末端和C末端缺失对其表达和纯化的影响
机译:叶绿体ATP合酶的ε亚基:C末端缺失对酶活性和调控的影响。
机译:阵列比较基因组杂交技术检测Dubowitz综合征患者的染色体14q32.33染色体缺失
机译:在韩国X型X-联系的Agammaglobulinemia患者中鉴定Bruton酪氨酸激酶基因中的突变,包括新的基因组重排,导致大缺失,导致大缺失