这是《临床遗传学》的网页。
临床遗传学研究，证明遗传因素在本病的发生中起一定的作用。
Clinical Genetics, proof of genetic factors in the occurrence of the disease play a role.
扎瓦斯这番评说源于与帕尔·比林斯的争论，后者是加州大学教授，也是临床遗传学专家，比林斯教授坚决反对任何关于克隆人的计划。
The remarks from Zavos came during a debate with Dr. Paul r. Billings, a University of California professor and an expert on clinical genetics, who bluntly rejected any plans to clone humans.
不过接下来的十年里可能会开展临床试验，鲍登如是说，他现在与Eos公司合作，该公司旨在用光遗传学治疗失明。
However, clinical trials may begin in the next decade, says Boyden, who is involved in a company, Eos, that aims to use optogenetics to treat blindness.
他的回答写在2005年的一篇题目为“多数”的论文中，其论点是：从新药的临床实验到前沿的遗传学研究，生物医学的研究中充满了错误结论。
His answer, in a 2005 paper: "the majority." From clinical trials of new drugs to cutting-edge genetics, biomedical research is riddled with incorrect findings, he argued.
我们可以在临床开发中采用遗传学进行患者分层。
We can use genetics to stratify patients in clinical development.
在细胞遗传学的临床与科学研究中，染色体分析是一项很重要的任务。
During the clinical and scientific research of cell genetics, the analysis of chromosome is an important task.
学习课程包括遗传学，免疫学，临床肿瘤学，分子疗法及相关学科。
Courses of study include genetics, immunology, clinical oncology, molecular therapeutics, and related subjects.
目的：了解中国人群中类脂蛋白沉积症(LP)的临床表型和遗传学特点。
Objective: To explore the clinical and genetic features of lipoid proteinosis (LP) in Chinese population.
目的探讨良性家族性新生儿惊厥(bfnc)的临床特征及遗传学特点。
Objective To explore the clinical and genetic characteristics of benign familial neonatal convulsion (BFNC).
方法：采用临床、实验室检查方法对3例患儿进行详细的体检，并分析导致出现牙根发育不良表型的遗传学因素。
METHODS: 3 children with hypoplasia of teeth were examined and analyzed carefully by clinical examination and laboratory test to find the genetic factors.
第二十六条从事医学技术鉴定的人员，必须具有临床经验和医学遗传学知识，并具有主治医师以上的专业技术职务。
Personnel engaged in medical technical appraisement must have clinical experience medical genetic knowledge and the professional title of physician-in-charge or above.
目的探讨急性白血病合并严重血小板增多症的细胞遗传学特点及其临床和实验室特征。
Objective To investigate the cytogenetic features as well as clinical and laboratory criteria of acute leukemia complicated with severe thrombocytosis.
我们报道了11例成年起病的亚历山大病详细的临床和基因数据，进行了为期4年多的观察，并回顾了先前报道的25例通过遗传学证实的成年起病的亚历山大病。
We report detailed clinical and genetic data of 11 cases of AOAD, observed over a 4-year period, and a review of the previously reported 25 cases of genetically confirmed AOAD.
ASS1是唯一已知与1型瓜氨酸血症相关的基因，ASS1的分子遗传学检测在临床就有提供。
Molecular genetic testing of ASS1, the only gene known to be associated with citrullinemia type I, is clinically available.
在前三项研究中，基于就诊时的临床表现与白血病细胞遗传学特点，选择治疗方案。
In the first three studies, treatment selection was based on presenting clinical features and leukemic cell genetics.
目的：了解炎症性肠病药物遗传学的现状，为该类药物在临床的合理应用提供参考。
OBJECTIVE: to investigate status quo of pharmacogenetics of inflammatory bowel disease (IBD), in order to provide some references for rational use of such kinds of drugs in the clinic.
为避免误诊以及不恰当的治疗方案，需密切联系临床、组织学、免疫表型和遗传学特征。
Careful correlation of clinical, histologic, immunophenotypic, and genetic features is required to avoid misdiagnosis and inappropriate treatment.
提示细胞遗传学对自发流产夫妇的临床诊断有很重要价值。
This paper showed that cytogenetics analysis is important for diagnosing the cases with spontaneous abortion.
FISH技术在肿瘤生物学研究及临床细胞遗传学、出生前诊断等被广泛应用。
Making the most of M-FISH techniques in cancer research and preimplantation genetic diagnostics.
这一关于神经遗传学的简单指南解密了这一领域的海量信息因此读者能够区分关键的临床特征并了解其处理选择。
This simple guide to neurogenetics demystifies the overwhelming amount of information on the subject so you can identify key clinical features and understand your management options.
结论：由npm 1,FLT3,CEBPA，和MLL基因的突变状态所界定的基因型与细胞遗传学正常的急性髓细胞白血病患者的临床治疗结局之间存在相关性。
Conclusions Genotypes defined by the mutational status of NPM1, FLT3, CEBPA, and MLL are associated with the outcome of treatment for patients with cytogenetically normal AML.
报告基因显像技术是分子影像学中重要的显像技术，其可对多种不同的生物学和分子遗传学过程进行显像，有望更快地应用于临床。
Reporter gene imaging is an important imaging technique in molecular imaging, which can image various biological and genetical processes. It has a potential in clinical application.
目的探明蒙古族一大家系牙本质发育不全症的临床特点和遗传学基础。
Objective To decipher the clinical characteristics and genetic bases of Dentinogenesis imperfecta type II in a large Mongolian family.
临床年度回顾三：吸烟、肺疾病的遗传学和慢性阻塞性肺疾病对肺康复、呼吸器官的健康的影响。
Clinical year in review III: pulmonary rehabilitation, respiratory health effects of smoking, genetics of lung disease, and chronic obstructive pulmonary disease.
我们报道16例经分子遗传学确诊的原发性肾脏滑膜肉瘤病例的临床病理学及免疫组织化学特征。
We report the clinicopathologic and immunohistochemical features of 16 cases of genetically confirmed primary synovial sarcoma of the kidney.
增加了原始细胞小于2 0 %伴有遗传学改变的特殊类型，更贴近于临床指标。
It increases a special type where myeloblast count is lower than 20% and is companied by genetic change. This is more close to clinical indexes.
目的分析儿童支气管典型类癌的临床病理学特征及细胞遗传学基础，探讨其诊断、治疗及预后。
Objective To analyze the clinicopathological characteristics and cytogenetic basis of bronchial typical carcinoid in children, and to investigate its diagnosis, treatment and prognosis.
目的了解国人遗传性非息肉病性结直肠癌（HNPCC）的临床病理及分子遗传学特征。
Objective To investigate the clinicopathological and molecular genetic characteristics of Chinese hereditary nonpolyposis colorectal cancer (HNPCC) pedigrees.
目的了解国人遗传性非息肉病性结直肠癌（HNPCC）的临床病理及分子遗传学特征。
Objective To investigate the clinicopathological and molecular genetic characteristics of Chinese hereditary nonpolyposis colorectal cancer (HNPCC) pedigrees.
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