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1
المؤلفون: M. Mannens, J.M.N. Hoovers, E. Redeker, M. Verjaal, A.P. Feinberg, P. Little, M. Boavida, N. Coad, M. Steenman, J. Bliek, N. Niikawa, H. Tonoki, Y. Nakamura, E.G. de Boer, R.M. Slater, R. John, J.K. Cowell, C. Junien, I. Henry, N. Tommerup, R, Weksberg, S.M. Pueschel, N.J. Leschot, A. Westerveld
المصدر: European Journal of Human Genetics. 2:3-23
مصطلحات موضوعية: Male, Parents, Beckwith-Wiedemann Syndrome, Beckwith–Wiedemann syndrome, Gene Expression, Trisomy, Chromosomal translocation, Biology, Methylation, Wilms Tumor, Translocation, Genetic, Sex Factors, Insulin-Like Growth Factor II, Neoplastic Syndromes, Hereditary, Chromosome regions, Genetics, medicine, Humans, Insulin, Genes, Tumor Suppressor, Imprinting (psychology), Child, Gene, In Situ Hybridization, Fluorescence, Genetics (clinical), Chromosome Aberrations, Chromosomes, Human, Pair 11, Breakpoint, Chromosome Mapping, Karyotype, DNA, medicine.disease, Pedigree, Karyotyping, Female, Polymorphism, Restriction Fragment Length
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2
المؤلفون: J.K. Cowell
المصدر: European Journal of Cancer. 29:1348
مصطلحات موضوعية: Cancer Research, medicine.medical_specialty, Oncology, business.industry, Molecular genetics, Medicine, Computational biology, business
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3Academic Journal
المؤلفون: A. Beghini, I. Magnani, G. Roversi, A.M. Fuhrman Conti, L. Larizza, T. Piepoli, S. Di Terlizzi, R. F. Moroni, B. Pollo, J. K. Cowell, G. Finocchiaro
المساهمون: A. Beghini, I. Magnani, G. Roversi, T. Piepoli, S. Di Terlizzi, R.F. Moroni, B. Pollo, A.M. Fuhrman Conti, J.K. Cowell, G. Finocchiaro, L. Larizza
مصطلحات موضوعية: Glioma, Intrachromosomal amplification, MARK4, Neural progenitor, Upregulation and overexpression, Wnt pathway, Settore MED/03 - Genetica Medica
Relation: info:eu-repo/semantics/altIdentifier/pmid/12735302; info:eu-repo/semantics/altIdentifier/wos/WOS:000182569000006; volume:22; issue:17; firstpage:2581; lastpage:2591; numberofpages:11; journal:ONCOGENE; http://hdl.handle.net/2434/192063; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0038530985