国际学生入学条件
Completed or be nearing the completion of a Bachelor of Science degree, a B+ average or higher both cumulatively and in the final year of a B.Sc. degree to be considered for our M.Sc. program, an A- average or higher both cumulatively and in the final year in their M.Sc. or B.Sc. to be considered for our Ph.D. program. TOEFL: Paper-Based Test and TWE- Overall Score 580 TWE: 5, Internet-Based Test (IBT): 93, Writing/Speaking: 22. IELTS: Minimum required score: 7.0 (Academic)with at least 6.5 for each component.
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IDP—雅思考试联合主办方
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雅思考试总分
7.0
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雅思考试指南
- 雅思总分:7
- 托福网考总分:93
- 托福笔试总分:580
- 其他语言考试:The Certificate of Proficiency in English (COPE) Required score: 76 (with at least 22 in each component and 32 in the writing component). MELAB: 85
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申请截止日期: 请与IDP顾问联系以获取详细信息。
课程简介
分子遗传学系由医学大楼管理,有近100名教职员工,其实验室位于医学大楼内
MoGen researchers studying Genetic Models of Development and Disease aim to understand how the instructions required to produce a complex multicellular organism are encoded in the genome, interpreted during embryonic development, and how errors in their implementation underlie diverse implementations pathologies, including many types of cancer. How a single cell, the fertilized egg, develops into an individual that may comprise trillions of cells has fascinated observers since its discovery. Over the past 40 years, phenomenal advances with genetic analysis and molecular biology have revealed many of the mechanisms that lay out plans of the developing body, specify the identities of different cell types, and pattern tissues and organs throughout the body. One of the striking lessons to emerge from such studies is that a small number of well-conserved regulatory pathways repeatedly act during development, in different contexts, and in organisms ranging from simple invertebrates to humans, to control decisions about cell fate, tissue growth, pattern formation, and morphogenesis. Consequently, discoveries about the workings of these pathways in simple, highly tractable organisms can readily be applied to investigate the development and genetic disease in more complex ones, including humans.
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