机译:墨西哥先天性输精管缺失患者CFTR基因的分子筛选
Genomic of Complex Diseases Laboratoy, Instituto Nacional de Medicina Genomica, SS, Mexico City, Mexico. ,Programa Institucional de Biomedicina Molecular, ENMyH-IPN, Mexico City, Mexico;
Genomic of Complex Diseases Laboratoy, Instituto Nacional de Medicina Genomica, SS, Mexico City, Mexico;
Department of Andrology, Instituto Nacional de Perinatologia, Mexico City, Mexico;
Genomic of Complex Diseases Laboratoy, Instituto Nacional de Medicina Genomica, SS, Mexico City, Mexico;
Subsecretaria de Salud del Distrito Federal, Mexico City, Mexico;
Genomic of Complex Diseases Laboratoy, Instituto Nacional de Medicina Genomica, SS, Mexico City, Mexico;
Genomic of Complex Diseases Laboratoy, Instituto Nacional de Medicina Genomica, SS, Mexico City, Mexico;
Genomic of Complex Diseases Laboratoy, Instituto Nacional de Medicina Genomica, SS, Mexico City, Mexico. ,Genomics Sciences Program, Universidad Autonoma de la Cd. de Mexico, Mexico City, Mexico.,Instituto National de Medicina Gendmica Periferico Sur 4124, Torre Zafiro II, 6° piso Col. Jardines del Pedregal Mexico City CP 01900 Mexico;
机译:埃及先天性双侧输精管缺失患者CFTR基因的分子筛查:初步研究
机译:扩大中国先天性患者患者的表型和遗传谱轴承CFTR CFTR CFTR和ADGRG 2 ADGRG ADGRG 2等位基因
机译:印度先天性输精管缺失患者CFTR基因突变的异质光谱及其与囊性纤维化遗传修饰因子的关系
机译:复杂的极化和光谱技术在卵巢癌患者血浆诊断中的初步分子遗传筛选
机译:先天性心脏病患者的稀有拷贝数变异确定了左右模式中的新基因
机译:先天性输精管缺失的患者的CFTR基因变异。
机译:22对葡萄牙人先天性输精管缺失的患者进行完整的CFTR基因筛选