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1دورية أكاديمية
المؤلفون: Tahir Zaib, Wei Ji, Komal Saleem, Guangchen Nie, Chao Li, Lin Cao, Baijun Xu, Kexian Dong, Hanfei Yu, Xuguang Hao, Yan Xue, Shuhan Si, Xueyuan Jia, Jie Wu, Xuelong Zhang, Rongwei Guan, Guohua Ji, Jing Bai, Feng Chen, Yong Liu, Wenjing Sun, Songbin Fu
المصدر: BMC Medical Genetics, Vol 20, Iss 1, Pp 1-9 (2019)
مصطلحات موضوعية: SPD1, HOXD13, Whole genome sequencing, Variable expressivity, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1471-2350
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2
المؤلفون: HangLong Li, Qiang Zhao, ShuHan Si, DongKai Wu
المصدر: Frontiers in Gastroenterology. 1
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fea2384fb1d3217edc2aad7444bad62
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3
المؤلفون: Shuhan Si, Jie Wu, Siqi Zhu, Songbin Fu, Kexian Dong, Qian Qin, Wenjing Sun, Wei Ji, Xueyuan Jia, Chunhui Zhang, Tahir Zaib, Yusi Wang, Lidan Xu, Hanfei Yu, Komal Saleem
المصدر: Bioscience Reports. 40
مصطلحات موضوعية: 0301 basic medicine, Sanger sequencing, In silico, Biophysics, Microsatellite instability, Cell Biology, Biology, medicine.disease, MLH1, Biochemistry, digestive system diseases, Lynch syndrome, 03 medical and health sciences, symbols.namesake, 030104 developmental biology, 0302 clinical medicine, Germline mutation, 030220 oncology & carcinogenesis, medicine, symbols, Cancer research, DNA mismatch repair, Molecular Biology, Exome sequencing
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4
المؤلفون: Yong Liu, Guohua Ji, Jie Wu, Rongwei Guan, Hao Xuguang, Songbin Fu, Tahir Zaib, Jing Bai, Yan Xue, Feng Chen, Lin Cao, Wenjing Sun, Shuhan Si, Guangchen Nie, Xuelong Zhang, Baijun Xu, Hanfei Yu, Chao Li, Kexian Dong, Wei Ji, Komal Saleem, Xueyuan Jia
المصدر: BMC Medical Genetics
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-9 (2019)مصطلحات موضوعية: 0301 basic medicine, Male, lcsh:Internal medicine, China, Heterozygote, lcsh:QH426-470, 030105 genetics & heredity, Biology, 03 medical and health sciences, Gene Duplication, Gene duplication, Variable expressivity, Genetics, medicine, Humans, 1000 Genomes Project, lcsh:RC31-1245, Child, Exome, Genetics (clinical), Homeodomain Proteins, HOXD13, Exons, SPD1, medicine.disease, Synpolydactyly, Human genetics, Pedigree, lcsh:Genetics, 030104 developmental biology, Whole genome sequencing, Mutation (genetic algorithm), Mutation, Mutation testing, Female, Syndactyly, Research Article, Transcription Factors
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المؤلفون: Zaib, Tahir, Ji, Wei, Komal Saleem, Guangchen Nie, Li, Chao, Cao, Lin, Baijun Xu, Kexian Dong, Hanfei Yu, Xuguang Hao, Xue, Yan, Shuhan Si, Xueyuan Jia, Wu, Jie, Xuelong Zhang, Rongwei Guan, Guohua Ji, Bai, Jing, Chen, Feng, Liu, Yong, Wenjing Sun, Songbin Fu
مصطلحات موضوعية: body regions, education, humanities
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7768a3f66933e2e5a52d6104e1075a66
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6
المؤلفون: Kexian Dong, Jing Bai, Lin Cao, Jie Wu, Rongwei Guan, Yong Liu, Guohua Ji, Hanfei Yu, Wenjing Sun, Yan Xue, Guangchen Nie, Chao Li, Wei Ji, Komal Saleem, Shuhan Si, Hao Xuguang, Xueyuan Jia, Tahir Zaib, Songbin Fu, Baijun Xu, Xuelong Zhang, Feng Chen
المصدر: Meta Gene.
مصطلحات موضوعية: Genetics, Exon, HOXD13 Gene, Base pair, Gene duplication, medicine, Chinese family, Biology, medicine.disease, Genetics (clinical), Synpolydactyly
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7دورية أكاديمية
المؤلفون: Saleem, Komal, Zaib, Tahir, Wei Ji, Chunhui Zhang, Qian Qin, Yusi Wang, Lidan Xu, Hanfei Yu, Siqi Zhu, Kexian Dong, Shuhan Si, Xueyuan Jia, Jie Wu, Songbin Fu, Wenjing Sun
المصدر: Bioscience Reports; Jun2020, Vol. 40 Issue 6, p1-14, 14p