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1دورية أكاديمية
المؤلفون: Huang, Xin, Chen, Chang, Lin, Yan, Wang, Changjun, Zhou, Xingtong, Xu, Ying, Sun, Qiang, Zhou, YidongAff1, IDs10549024073417_cor8
المصدر: Breast Cancer Research and Treatment. 206(3):653-666
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2كتاب إلكتروني
المؤلفون: Li, Lin-FengAff3, Olsen, Kenneth M.Aff4
المساهمون: Rajora, Om P., Editor-in-ChiefAff1, Aff2
المصدر: Population Genomics: Crop Plants. :87-111
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3دورية أكاديمية
المؤلفون: Wang, YananAff1, IDs41065024003124_cor1, Chang, Yujie, Gao, Mingya, Zang, Weiwei, Liu, Xiaofei
المصدر: Hereditas. 161(1)
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4دورية أكاديمية
المؤلفون: Arango-Ibañez, Juan PabloAff1, Aff2, Parra-Lara, Luis GabrielAff1, Aff2, Zambrano, Ángela R., Rodríguez-Rojas, Lisa XimenaAff1, Aff4, IDs13053023002722_cor4
المصدر: Hereditary Cancer in Clinical Practice. 22(1)
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5دورية أكاديمية
المؤلفون: Yue, XingAff1, IDs12033023007618_cor1, Luo, Yaheng, Wang, Jing, Huang, DebinAff1, IDs12033023007618_cor4
المصدر: Molecular Biotechnology. 66(3):467-474
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6دورية أكاديمية
المؤلفون: Christopher J. Yoon, Chang Hyun Nam, Taewoo Kim, Jeong Seok Lee, Ryul Kim, Kijong Yi, June-Young Koh, Jiye Kim, Hyein Won, Ji Won Oh, Obi L. Griffith, Malachi Griffith, Joohon Sung, Tae Yeul Kim, Duck Cho, Ji Seon Choi, Young Seok Ju
المصدر: HGG Advances, Vol 5, Iss 3, Pp 100301- (2024)
مصطلحات موضوعية: monochorionic dizygotic twins, chimera, single-cell sequencing, lineage tracing, de novo mutation, Genetics, QH426-470
وصف الملف: electronic resource
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7دورية أكاديمية
المؤلفون: Chow, Julie C, Hormozdiari, Fereydoun
المصدر: Journal of Autism and Developmental Disorders. 53(3)
مصطلحات موضوعية: Education, Health Sciences, Psychology, Neurosciences, Genetics, Aetiology, 2.1 Biological and endogenous factors, Humans, Mutation, Autism Spectrum Disorder, Neurodevelopmental Disorders, Phenotype, De novo mutation, Early prediction, Neural network, Likely gene-disruptive, Missense, Psychology and Cognitive Sciences, Developmental & Child Psychology, Health sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/12w832p5
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8دورية أكاديمية
المؤلفون: Liu, XianyangAff1, Aff2, Aff3, Meng, JiayuAff1, Aff2, Aff3, Aff4, Liao, XingyunAff1, Aff2, Aff3, Aff5, Liu, YusenAff1, Aff2, Aff3, Zhou, QianAff1, Aff2, Aff3, Xu, ZongrenAff1, Aff2, Aff3, Yin, Shuming, Cao, QingfengAff1, Aff2, Aff3, Su, GuannanAff1, Aff2, Aff3, He, SiyuanAff1, Aff2, Aff3, Li, WanqianAff1, Aff2, Aff3, Wang, XiaotangAff1, Aff2, Aff3, Wang, GuoqingAff1, Aff2, Aff3, Li, Dali, Yang, PeizengAff1, Aff2, Aff3, IDs41423023010889_cor15, Hou, ShengpingAff1, Aff2, Aff3, Aff7, IDs41423023010889_cor16
المصدر: Cellular & Molecular Immunology. 20(11):1379-1392
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9دورية أكاديمية
المؤلفون: Yanan Wang, Yujie Chang, Mingya Gao, Weiwei Zang, Xiaofei Liu
المصدر: Hereditas, Vol 161, Iss 1, Pp 1-8 (2024)
مصطلحات موضوعية: Albinism, OCA2 gene, De novo mutation, Compound heterozygous mutations, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1601-5223
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10دورية أكاديمية
المؤلفون: Juan Pablo Arango-Ibañez, Luis Gabriel Parra-Lara, Ángela R. Zambrano, Lisa Ximena Rodríguez-Rojas
المصدر: Hereditary Cancer in Clinical Practice, Vol 22, Iss 1, Pp 1-5 (2024)
مصطلحات موضوعية: Li Fraumeni syndrome, TP53, P53, De novo mutation, Advanced paternal age, Severe phenotype, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1897-4287