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المؤلفون: Jennifer Skaug, Karen W. Gripp, Luis Armengol, Sanaa Choufani, Lisa G. Shaffer, Ikuko Teshima, Dorota Kwasnicka, Elena Belloni, Peter M. Kroisel, Qing Zhang, Miguel Angel Pujana, David Chitayat, Hartmut Döhner, Sarah J. Mould, David G. Oscier, Andrew P. Boright, Steven R. Herrick, Peter Szatmari, Simone Gentles, May Haddad, Lucy R. Osborne, Azra H. Ligon, J. Craig Venter, Karl Heinz Grzeschik, James F. Gusella, Emiko Kanematsu, Junjun Zhang, Jeffrey R. MacDonald, Eitan Zlotorynski, Zhongwu Lai, Anne W. Higgins, Zhiping Gu, Theresa A. Grebe, Johanna M. Rommens, Barbara R. Pober, Stephen W. Scherer, Constantine C. Christopoulos, Pier Giuseppe Pelicci, Cynthia C. Morton, Anne M. Summers, Razi Khaja, Michael D. Wilson, Berge A. Minassian, Chantal Farra, Hyung Goo Kim, Ahmed Teebi, Elizabeth J.T. Winsor, Gudrun E. Moore, Nazneen Rahman, Heather L. Ferguson, John B. Vincent, Kazuhiko Nakabayashi, Henry H.Q. Heng, Batsheva Kerem, Wendy Roberts, Xiangqun H. Zheng, Jan M. Friedman, Martin Li, Francesco Lo-Coco, Susan Zeesman, Juha Kere, Richard J. Mural, Małgorzata J.M. Nowaczyk, Ben F. Koop, Jo Anne Herbrick, Bradley J. Quade, Alexander K. Hudek, Bridget A. Fernandez, Lap-Chee Tsui, Fu Lu, Peter W. Li, Gavin E. Duggan, Joseph Y. Cheung, Gail A. P. Bruns, Susan J. Kirkpatrick, Konstanze Döhner, Bruce R. Korf, Elaine H. Zackai, Xavier Estivill, Silvano Tosi, Rosanna Weksberg, Erwin Petek, Natalia T. Leach, Deborah R. Nusskern, Sarah R. Cox, Emmanuelle Lemyre, Andrew R. Carson, Cheryl Shuman, Mark Raymond Adams, Layla Parker-Katiraee
مصطلحات موضوعية: Williams Syndrome, Euchromatin, Congenital, Mice, Complementary, Gene Duplication, Neoplasms, Databases, Genetic, Genes, Overlapping, In Situ Hybridization, Fluorescence, In Situ Hybridization, Segmental duplication, Overlapping, Genetics, Chromosome 7 (human), Expressed Sequence Tags, Multidisciplinary, Chromosome Fragile Sites, Chromosome Mapping, Limb Deformities, Genetic Diseases, Animals, Autistic Disorder, Chromosome Aberrations, Chromosome Fragility, Chromosomes, Human, Pair 7, Computational Biology, Congenital Abnormalities, CpG Islands, DNA, Complementary, Genetic Diseases, Inborn, Genomic Imprinting, Humans, Limb Deformities, Congenital, Molecular Sequence Data, Mutation, Pseudogenes, RNA, Retroelements, Sequence Analysis, DNA, Pair 7, Sequence Analysis, Human, Sequence analysis, Genetic diseases, inborn - genetics, Chromosomal rearrangement, Biology, Article, Chromosomes, Fluorescence, Databases, Genetic, Chromosome 19, DNA, Inborn, Genes, Human genome, Chromosome 21, Chromosomes, human, pair 7 - genetics, Chromosome 22, Settore MED/15 - Malattie del Sangue
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1d5e41971c0fe03c12ca6bc3377b9c
http://hdl.handle.net/2108/162063 -
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المؤلفون: David G, Oscier, Anne C, Gardiner, Sarah J, Mould, Sharron, Glide, Zadie A, Davis, Rachel E, Ibbotson, Martin M, Corcoran, Robert M, Chapman, Peter W, Thomas, J Adrian, Copplestone, Jenny A, Orchard, Terry J, Hamblin
المصدر: Blood. 100(4)
مصطلحات موضوعية: Male, Analysis of Variance, Sex Characteristics, Chromosomes, Human, Pair 12, Membrane Glycoproteins, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 11, Immunoglobulin Variable Region, Trisomy, Genes, p53, Prognosis, ADP-ribosyl Cyclase 1, Antigens, Differentiation, Leukemia, Lymphocytic, Chronic, B-Cell, Survival Rate, Blotting, Southern, NAD+ Nucleosidase, Antigens, CD, Mutation, Humans, Female, ADP-ribosyl Cyclase, Immunoglobulin Heavy Chains, Gene Deletion, Proportional Hazards Models
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::9275a40804bc1f440317ce030376cd97
https://pubmed.ncbi.nlm.nih.gov/12149185