机译:受22季度缺失综合征影响的患者群体中的耳鼻喉科特征:一项单眼调查
Department of Translational Medical Sciences Pediatric sectionFederico II UniversityNaples Italy;
Department of Translational Medical Sciences Pediatric sectionFederico II UniversityNaples Italy;
Department of Advanced Biomedical SciencesFederico II UniversityNaples Italy;
Department of Advanced Biomedical SciencesFederico II UniversityNaples Italy;
Department of Translational Medical Sciences Pediatric sectionFederico II UniversityNaples Italy;
Department of Neurosciences Reproductive and Odontostomatological SciencesFederico II;
Department of Morphologic and Functional Diagnostics Radiotherapy and Legal MedicineFederico II;
Department of Translational Medical Sciences Pediatric sectionFederico II UniversityNaples Italy;
Department of Neurosciences Reproductive and Odontostomatological SciencesFederico II;
22q11.2 deletion syndrome; DiGeorge syndrome; ENT phenotype;
机译:受22季度缺失综合征影响的患者群体中的耳鼻喉科特征:一项单眼调查
机译:3-18岁捷克患者队队(NORIAMS-BEUREN-,NOUNAN-,NOONAN-和22Q11.2删除综合征的临床综合征
机译:扩大胎儿表型:患有确认的22Q11.2缺失综合征的患者队列的产前超声成像和围产期结果
机译:22Q11.2缺失综合征在调查白质改变的替代扩散各向异性措施
机译:遗传学的新面貌:医学界对提高患者满意度的教育。 22q11.2删除综合征和特纳综合征的比较。
机译:通过墨西哥原发性心面综合征的特征原位杂交检测到22q11.2缺失
机译:22Q11.2删除综合征的耳鼻喉科表现