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1دورية أكاديمية
المؤلفون: John Herriges, Cassandra Runke, Zoe Lewis, Lucilla Pizzo, Bradley Coe, Laura Conlin, Benjamin Hilton, Brynn Levy, Andrea Vaags, Shulin Zhang, Christa Martin, Erica Andersen
المصدر: Genetics in Medicine Open, Vol 1, Iss 1, Pp 100532- (2023)
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Cheen Euong Ang, Qing Ma, Orly L Wapinski, ShengHua Fan, Ryan A Flynn, Qian Yi Lee, Bradley Coe, Masahiro Onoguchi, Victor Hipolito Olmos, Brian T Do, Lynn Dukes-Rimsky, Jin Xu, Koji Tanabe, LiangJiang Wang, Ulrich Elling, Josef M Penninger, Yang Zhao, Kun Qu, Evan E Eichler, Anand Srivastava, Marius Wernig, Howard Y Chang
المصدر: eLife, Vol 8 (2019)
مصطلحات موضوعية: long non-coding RNA, induced neuronal cells, autism, genomics, Medicine, Science, Biology (General), QH301-705.5
وصف الملف: electronic resource
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3
المؤلفون: Momchil Nikolov, Lilian Antunes, Bradley Coe, Matthew B. Dobbs, Christina A. Gurnett, Ina E Amarillo, Brooke Sadler, Gabe Haller
المصدر: Journal of Medical Genetics. 57:851-857
مصطلحات موضوعية: Genetics, Clubfoot, Pseudoautosomal region, Chromosome, Aneuploidy, Biology, medicine.disease, Idiopathic short stature, Gene duplication, medicine, Copy-number variation, Exome, Genetics (clinical)
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4
المؤلفون: Brooke, Sadler, Gabe, Haller, Lilian, Antunes, Momchil, Nikolov, Ina, Amarillo, Bradley, Coe, Matthew B, Dobbs, Christina A, Gurnett
المصدر: Journal of Medical Genetics
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, DNA Copy Number Variations, complex traits, Short Stature Homeobox Protein, Gene Duplication, Chromosome Duplication, Exome Sequencing, copy-number, Humans, Paired Box Transcription Factors, Genetic Predisposition to Disease, genetics, aneuploidy, Child, Pseudoautosomal Regions, Infant, Middle Aged, Microarray Analysis, Pedigree, Clubfoot, Child, Preschool, molecular genetics, Copy-Number Variation, T-Box Domain Proteins
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5
المؤلفون: Cheen Euong, Ang, Qing, Ma, Orly L, Wapinski, ShengHua, Fan, Ryan A, Flynn, Qian Yi, Lee, Bradley, Coe, Masahiro, Onoguchi, Victor Hipolito, Olmos, Brian T, Do, Lynn, Dukes-Rimsky, Jin, Xu, Koji, Tanabe, LiangJiang, Wang, Ulrich, Elling, Josef M, Penninger, Yang, Zhao, Kun, Qu, Evan E, Eichler, Anand, Srivastava, Marius, Wernig, Howard Y, Chang
المصدر: eLife
مصطلحات موضوعية: Male, DNA Copy Number Variations, Mouse, Autism Spectrum Disorder, Neurogenesis, autism, Translocation, Genetic, genomics, Humans, Child, Neurons, induced neuronal cells, Chromosomes, Human, Pair 12, long non-coding RNA, Gene Expression Profiling, Cell Differentiation, Genetics and Genomics, Stem Cells and Regenerative Medicine, Pedigree, Neurodevelopmental Disorders, Mutation, Chromosomes, Human, Pair 5, Female, RNA, Long Noncoding, Research Article, Human