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المؤلفون: Antanaviciute, A, Baquero-Perez, B, Watson, CM, Harrison, SM, Lascelles, C, Crinnion, L, Markham, AF, Bonthron, DT, Whitehouse, A, Carr, IM
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a166da136105180a26f132404bdaabc3
https://ora.ox.ac.uk/objects/uuid:e4e1943e-daab-48dd-a5d7-4fc12908d111 -
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المؤلفون: Diggle, CP, Martinez-Garay, I, Molnar, Z, Brinkworth, MH, White, E, Fowler, E, Hughes, R, Hayward, BE, Carr, IM, Watson, CM, Crinnion, L, Asipu, A, Woodman, B, Coletta, PL, Markham, AF, Dear, TN, Bonthron, DT, Peckham, M, Morrison, EE, Sheridan, E, Guo, X
المصدر: PloS One. 12(4)
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المؤلفون: Picton H M, Huntriss J, Hodge D, Judson H, De Vos M, Hayward B E, Sheridan E, Bonthron DT
المصدر: BMC Genetics, Vol 4, Iss 1, p 2 (2003)
مصطلحات موضوعية: autozygosity, hydatidiform mole, imprinting, oogenesis, Genetics, QH426-470
وصف الملف: electronic resource
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المؤلفون: Watson, CM, Crinnion, LA, Harrison, SM, Lascelles, C, Antanaviciute, A, Carr, IM, Bonthron, DT, Sheridan, E, Sharakhov, IV
المساهمون: Sharakhov, I
المصدر: PLoS ONE, Vol 11, Iss 6, p e0157075 (2016)
PLoS ONEمصطلحات موضوعية: 0301 basic medicine, lcsh:Medicine, 030105 genetics & heredity, Biochemistry, Chromosome Breakpoints, Genome Sequencing, lcsh:Science, Exome sequencing, Chromosomal inversion, Genetics, Sanger sequencing, Multidisciplinary, Mammalian Genomics, Chromosome Biology, Nucleotide Mapping, High-Throughput Nucleotide Sequencing, Genomics, Inversions, Chromosomal Aberrations, symbols, Female, Hand Deformities, Congenital, Sequence Analysis, Chromosomes, Human, Pair 7, Research Article, Foot Deformities, Congenital, Locus (genetics), Biology, Research and Analysis Methods, DNA sequencing, Chromosomes, 03 medical and health sciences, symbols.namesake, Protein Domains, Genomic Medicine, Humans, Homeobox, Abnormalities, Multiple, Molecular Biology Techniques, Sequencing Techniques, Molecular Biology, Whole genome sequencing, Homeodomain Proteins, Chromosome 7, Breakpoint, Gene Mapping, lcsh:R, Infant, Newborn, Biology and Life Sciences, Proteins, Sequence Analysis, DNA, Cell Biology, Chromosome Pairs, 030104 developmental biology, Animal Genomics, Urogenital Abnormalities, Chromosome Inversion, lcsh:Q, Sequence Alignment
وصف الملف: application/pdf
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المؤلفون: Mirzaa, GM, Parry, DA, Fry, AE, Giamanco, KA, Schwartzentruber, J, Vanstone, M, Logan, CV, Roberts, N, Johnson, CA, Singh, S, Kholmanskikh, SS, Adams, C, Hodge, RD, Hevner, RF, Bonthron, DT, Braun, KPJ, Faivre, L, Rivière, J-B, St-Onge, J, Gripp, KW, Mancini, GMS, Pang, K, Sweeney, E, Van Esch, H, Verbeek, N, Wieczorek, D, Steinraths, M, Majewski, J, FORGE Canada Consortium, Boycott, KM, Pilz, DT, Ross, ME, Dobyns, WB, Sheridan, EG
المصدر: Nature genetics, vol 46, iss 5
مصطلحات موضوعية: endocrine system, Molecular Sequence Data, Medical and Health Sciences, Fluorescence, Mice, Animals, Humans, Site-Directed, Cyclin D2, 2.1 Biological and endogenous factors, Exome, Aetiology, Pediatric, Microscopy, Base Sequence, Blotting, Syndrome, DNA, Biological Sciences, FORGE Canada Consortium, Immunohistochemistry, Megalencephaly, Malformations of Cortical Development, Polydactyly, Electroporation, HEK293 Cells, Bromodeoxyuridine, Mutagenesis, Female, Abnormalities, Multiple, Western, Sequence Analysis, Hydrocephalus, Developmental Biology
وصف الملف: application/pdf
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9دورية أكاديمية
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10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.