المؤلفون: Iwahiro ISOGAI, Masao KIMURA, Shin-ichi ITO, 伊藤 慎一, 木村 正雄, 磯貝 岩弘

المصدر: 日本畜産学会報 / Nihon Chikusan Gakkaiho. 1988, 59(9):822

المؤلفون: Iwahiro ISOGAI, Masao KIMURA, Shin-ichi ITO, 伊藤 慎一, 木村 正雄, 磯貝 岩弘

المصدر: 日本畜産学会報 / Nihon Chikusan Gakkaiho. 1988, 59(9):801

المؤلفون: Wenyi Wang, Gang Peng, Yu Fan

المصدر: PLoS Computational Biology
PLoS Computational Biology, Vol 10, Iss 10, p e1003880 (2014)

مصطلحات موضوعية: Heredity, Computer science, Genetic Linkage, computer.software_genre, Computer graphics, 0302 clinical medicine, Software, Mathematical and Statistical Techniques, Image Processing, Computer-Assisted, Probability Estimation, Autosomal Linkage, Graphics, lcsh:QH301-705.5, 0303 health sciences, Ecology, High-Throughput Nucleotide Sequencing, Pedigree, Computational Theory and Mathematics, Sex Linkage, X-Linked Traits, Modeling and Simulation, Data mining, Central processing unit, Algorithms, Research Article, Bayesian Method, Graphics processing unit, Markov model, Research and Analysis Methods, 03 medical and health sciences, Cellular and Molecular Neuroscience, Genetic model, Genetics, Computer Graphics, Point Mutation, Humans, Family, Molecular Biology, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Models, Genetic, business.industry, Bayesian network, Biology and Life Sciences, Computational Biology, Genetic Variation, Sequence Analysis, DNA, lcsh:Biology (General), Mutation, business, computer, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f60457121ebf62fa368a8a3a20e38af
http://europepmc.org/articles/PMC4214554

المؤلفون: Haghighi, Alireza, Tiwari, Amit, Piri, Niloofar, Nürnberg, Gudrun, Saleh-Gohari, Nasrollah, Haghighi, Amirreza, Neidhardt, John, Nürnberg, Peter, Berger, Wolfgang

مصطلحات موضوعية: Biology and life sciences, Computational Biology, Genome Analysis, Transcriptome Analysis, Next-Generation Sequencing, Genetics, Genomics, Human Genomics, Heredity, Genetic Linkage, Autosomal Linkage, Chromosomal Inheritance, Homozygosity, Mutation, Frameshift Mutation, Molecular Genetics, Molecular biology, Molecular biology techniques, Sequencing techniques, DNA sequencing, Dideoxy DNA sequencing, High Throughput Sequencing, Medicine and Health Sciences, Ophthalmology, Retinal Disorders, Retinal Degeneration, Visual Impairments, Blindness, Myopia, Inherited Eye Disorders

وصف الملف: application/pdf

Relation: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231049/pdf/; PLoS ONE; Haghighi, Alireza, Amit Tiwari, Niloofar Piri, Gudrun Nürnberg, Nasrollah Saleh-Gohari, Amirreza Haghighi, John Neidhardt, Peter Nürnberg, and Wolfgang Berger. 2014. “Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome.” PLoS ONE 9 (11): e112747. doi:10.1371/journal.pone.0112747. http://dx.doi.org/10.1371/journal.pone.0112747.; http://nrs.harvard.edu/urn-3:HUL.InstRepos:13454758

الاتاحة: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13454758
https://doi.org/10.1371/journal.pone.0112747

المؤلفون: Xiong, Dong-Hai, Wang, Jin-Tang, Wang, Wei, Guo, Yan-Fang, Xiao, Peng, Shen, Hui, Jiang, Hui, Chen, Yuan, Deng, Hongyi, Drees, Betty, Recker, Robert R., Deng, Hong-Wen

المصدر: Human Biology 79(6):593-608. 2007