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[会议论文] 作者：Zishui Fang,Weiying Jiang,Shiyan Xu,
来源：2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份：2014
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[会议论文] 作者：Zishui Fang,Shiyan Xu,Weiying Jiang,
来源：广东省遗传学会第九届代表大会暨学术研讨会 年份：2014
Polycystic kidney disease (PKD) includes autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD), which has always been associated with a high pr...
Genetic detection of a pedigree with Hypochondroplasia from south China and identification of a nove
[会议论文] 作者：Dongwei Guo,Rong Li,Yibin Guo,Weiying Jiang,
来源：2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份：2014
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Genetic detection of a pedigree with Hypochondroplasia from south China and identification of a nove
[会议论文] 作者：Dongwei Guo,Rong Li,Yibin Guo,Weiying Jiang,
来源：2014全球华人遗传学大会暨全国第十三次医学遗传学学术会议 年份：2014
Objective: To reveal the molecular genetics mechanism of a pedigree with hypochondroplasia (HCH) from south China and create the necessary prerequisite of its future prenatal gene diagnosis.Methods: O...
[会议论文] 作者：Yibin Guo,Jingxin Pan,Dongwei Guo,Yan Zhao,Weiying Jiang,Xinyuan Liu,
来源：广东省遗传学会第九届代表大会暨学术研讨会 年份：2014
Objective To establish effective and specific methods of preimplantation genetic diagnosis so as to pave the way to implement the first PGD case of Morquio...
Molecular Diagnosis of a Chinese Pedigree with Alpha-Mannosidosis and Identification of a Novel Miss
[会议论文] 作者：Xiaoyun Wu,Yibin Guo,Jingxin Pan,Jia Tang,Yang Ai,Weiying Jiang,
来源：第十二次全国医学遗传学学术会议 年份：2013
Objective The purpose of this study was to research the molecular genetic mechanism of alpha-mannosidosis, to reveal the relationship between the genotype and phenotype, and to provide a prerequisite...
[会议论文] 作者：Zhihui He,Juan Chen,Shiyan Xu,Shufeng Chen,Hongyi Li,Yibin Guo,Weiying Jiang,
来源：2011中国遗传学会大会 年份：2011
@@ Hemophilia A is an X-linked recessive hereditary hemorrhagic disease, with an incidence of 1/5000 males. Mutation of Anti-hemophilic globulin A (AHG) causes...
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