打印 科室与专家门诊 妙佑医疗国际是美国规模最大、经验最丰富的医疗机构之一，在亚利桑那州、佛罗里达州和明尼苏达州都设有院区。我们的工作人员涉及数十种专业，通过齐心协力确保高品质治疗与成功康复。 有相关专长的科室 Early-Onset Colorectal Cancer Group 临床基因组学科 妇产科 早发性和遗传性消化道癌症项目 肾病和高血压 行此手术的医生 编辑搜索过滤条件 close 缩小搜索范围 根据地点 Rochester, MN 按姓氏 查找姓氏以该字母开头的医生 A A 未找到姓氏以该字母开头的医生 B B 未找到姓氏以该字母开头的医生 C C 未找到姓氏以该字母开头的医生 D D 未找到姓氏以该字母开头的医生 E E 未找到姓氏以该字母开头的医生 F F 查找姓氏以该字母开头的医生 G G 未找到姓氏以该字母开头的医生 H H 未找到姓氏以该字母开头的医生 I I 未找到姓氏以该字母开头的医生 J J 未找到姓氏以该字母开头的医生 K K 未找到姓氏以该字母开头的医生 L L 未找到姓氏以该字母开头的医生 M M 查找姓氏以该字母开头的医生 N N 未找到姓氏以该字母开头的医生 O O 未找到姓氏以该字母开头的医生 P P 未找到姓氏以该字母开头的医生 Q Q 未找到姓氏以该字母开头的医生 R R 主动 查找姓氏以该字母开头的医生 S S 未找到姓氏以该字母开头的医生 T T 未找到姓氏以该字母开头的医生 U U 未找到姓氏以该字母开头的医生 V V 未找到姓氏以该字母开头的医生 W W 未找到姓氏以该字母开头的医生 X X 未找到姓氏以该字母开头的医生 Y Y 未找到姓氏以该字母开头的医生 Z Z 重置所有过滤器 搜索提示 给搜索词加引号。 即使搜索栏没有显示自动建议，也请点击“搜索”，您或许仍然可以获得结果。 显示$起始范围 - $结束范围/源自可用$可用医生 姓氏首字母: S Lisa A. Schimmenti, M.D. Pediatrician Medical Geneticist Rochester, MN 擅长领域： Genetic testing, Newborn screening, Genetic disorder, Retinitis pigmentosa, Hearing loss, Eye problem, Hearing loss in ...children, Bardet-Biedl syndrome 显示更多擅长领域 针对 Lisa A. Schimmenti, M.D. 研究妙佑医疗国际的个性化医疗中心提供个性化医疗服务，包括为了确定每个人独特的疾病易感性而进行的基因研究，制定预防措施，实现促进健康的靶向治疗。 妙佑医疗国际一直通过众多研究项目坚定致力于遗传学和基因组学研究。下面是一些案例： 妙佑医疗国际的结肠癌家族注册登记库项目参加了一个致力于加深对结肠直肠癌风险因素理解的国际联盟。 妙佑医疗国际生物样本库收集捐献的血液样本，用于研究，以更好地了解个人基因如何影响整体健康和保健状况。 文献请参阅美国国家医学图书馆检索服务系统 PubMed 所收录的妙佑医疗国际作者在基因检测领域的文献著述列表。 来自妙佑医疗国际员工 在 Mayo Clinic 治疗 申请预约 关于在 Mayo Clinic 治疗 July 02, 2022 打印 显示参考文献 National Library of Medicine. Help me understand genetics. Genetics Home Reference. https://ghr.nlm.nih.gov/primer. Accessed Feb. 13, 2017. Frequently asked questions about genetic testing. National Human Genome Research Institute. https://www.genome.gov/19516567/faq-about-genetic-testing/. Accessed Feb. 13, 2017. Genetic testing for hereditary cancer syndromes. National Cancer Institute. https://www.cancer.gov/about-cancer/causes-prevention/genetics/genetic-testing-fact-sheet. Accessed Feb. 13, 2017. Raby BA, et al. Genetic testing. http://www.uptodate.com/home. Accessed Feb. 13, 2017. Grody WW, et al. ACMG position statement on prenatal/preconception expanded carrier screening. Genetics in Medicine. 2013;15:482. Genetic testing. American Medical Association. https://www.ama-assn.org/content/genetic-testing. Accessed Feb. 13, 2017. Frequently asked questions. Prenatal genetic diagnostic tests. FAQ164. Pregnancy. American College of Obstetricians and Gynecologists. https://www.acog.org/-/media/For-Patients/faq164.pdf?dmc=1&ts=20161216T1208042192. Accessed Feb. 13, 2017. Breast cancer risk factors you cannot change. American Cancer Society. https://www.cancer.org/cancer/breast-cancer/risk-and-prevention/breast-cancer-risk-factors-you-cannot-change.html. Accessed Feb. 21, 2017. Medical review (expert opinion). Mayo Clinic, Jacksonville, Fla. Feb. 24, 2017. 相关 三 X 染色体综合征 不孕不育症 乳腺癌基因检测 亨廷顿病 侏儒症 先天性睾丸发育不全综合征 先天性肾上腺皮质增生症 共济失调 凝血因子 V 莱顿突变 副神经节瘤 努南综合征 原发性进行性失语症 唐氏综合征 嗜铬细胞瘤 囊性纤维化 地中海贫血 埃勒斯-当洛斯综合征 大疱性表皮松解症 威尔逊氏症 安格尔曼综合征 少精子症 尿崩症 布鲁加达综合征 戈谢病 扩张型心肌病 早老症 普拉德-威利综合征 林奇综合征 流产后怀孕 海绵状血管畸形 特纳综合征 男性不育症 男性性腺功能减退症 真性红细胞增多症 神经鞘瘤病 结肠息肉 绘制基因组信息 肌营养不良 肥厚型心肌病 肺高压 胸主动脉瘤 脉络丛癌 脑瘫 腓骨肌萎缩症 苯丙酮尿症（PKU） 血色素沉着症 视频：绒毛活检 迪格奥尔格综合征（22q11.2 缺失综合征） 遗传学与心肌病 长 QT 综合征 雷特综合征 非典型生殖器 颅缝早闭 马方综合征 骨髓纤维化 显示更多相关内容 Mayo Clinic 新闻 Mayo Clinic study sheds light on rare genetic disorder and blood cancers Mayo Clinic Q and A: Understanding carrier screening for family planning Mayo Clinic and Oxford Nanopore announce collaboration to advance precision medicine for cancer and genetic disorders Beyond BRCA1/2: Pinpointing the risk of inherited breast cancer genes Mayo Clinic's DNA study reveals BRCA1 mutations in 3 sisters, prompts life-changing decisions Understanding triple-negative breast cancer and its treatment A silent tumor, precancerous polyps and the power of genetic screening Comprehensive testing helps diagnose and manage rare genetic disorder Genomics study enrolls 100,000 participants Mayo's new 'omics' strategy leaps into the future New Mayo Clinic technology helps solve the unsolvable in rare disease diagnoses RegenBio Summit: Could a molecular scissors heal disease? 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