المؤلفون: Houlston, Richard S, Cheadle, Jeremy, Dobbins, Sara E, Tenesa, Albert, Jones, Angela M, Howarth, Kimberley, Spain, Sarah L, Broderick, Peter, Domingo, Enric, Farrington, Susan, Prendergast, James GD, Pittman, Alan M, Theodoratou, Evi, Smith, Christopher G, Olver, Bianca, Walther, Axel, Barnetson, Rebecca A, Churchman, Michael, Jaeger, Emma EM, Penegar, Steven, Barclay, Ella, Martin, Lynn, Gorman, Maggie, Mager, Rachel, Johnstone, Elaine, Midgley, Rachel, Niittymäki, Iina, Tuupanen, Sari, Colley, James, Idziaszczyk, Shelley, Thomas, Huw JW, Lucassen, Anneke M, Evans, D Gareth R, Maher, Eamonn R, Maughan, Timothy, Dimas, Antigone, Dermitzakis, Emmanouil, Cazier, Jean-Baptiste, Aaltonen, Lauri A, Pharoah, Paul, Kerr, David J, Carvajal-Carmona, Luis G, Campbell, Harry, Dunlop, Malcolm G, Tomlinson, Ian PM

المصدر: Nature Genetics. 42(11)

مصطلحات موضوعية: Prevention, Cancer, Genetics, Colo-Rectal Cancer, Human Genome, Digestive Diseases, Chromosome Mapping, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 12, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 3, Colorectal Neoplasms, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Male, Meta-Analysis as Topic, Odds Ratio, Oligonucleotide Array Sequence Analysis, Polymorphism, Single Nucleotide, Risk Assessment, COGENT Consortium, CORGI Consortium, COIN Collaborative Group, COINB Collaborative Group, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7r09g9scTest

المؤلفون: Buckley, Patrick G, Mantripragada, Kiran K, Díaz de Ståhl, Teresita, Piotrowski, Arkadiusz, Hansson, Caisa M, Kiss, Hajnalka, Vetrie, David, Ernberg, Ingemar T, Nordenskjöld, Magnus, Bolund, Lars, Sainio, Markku, Rouleau, Guy A, Niimura, Michihito, Wallace, Andrew J, Evans, D Gareth R, Grigelionis, Gintautas, Menzel, Uwe, Dumanski, Jan P

المصدر: Buckley , P G , Mantripragada , K K , Díaz de Ståhl , T , Piotrowski , A , Hansson , C M , Kiss , H , Vetrie , D , Ernberg , I T , Nordenskjöld , M , Bolund , L , Sainio , M , Rouleau , G A , Niimura , M , Wallace , A J , Evans , D G R , Grigelionis , G , Menzel , U & Dumanski , J P 2005 , ' Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and ....

مصطلحات موضوعية: Adaptor Proteins, Signal Transducing, Calcineurin, Chromosome Aberrations, Chromosome Mapping, Chromosomes, Human, Pair 22, Computational Biology, Diagnosis, Differential, Gene Dosage, Gene Rearrangement, Genes, Neurofibromatosis 2, Glutathione Transferase, Humans, Immunoglobulin lambda-Chains, Microarray Analysis, Mutation, Neurilemmoma, Phosphoproteins, Polymorphism, Genetic

الإتاحة: https://doi.org/10.1002/humu.20255Test
https://pure.au.dk/portal/da/publications/identification-of-genetic-aberrations-on-chromosome-22-outside-the-nf2-locus-in-schwannomatosis-and-neurofibromatosis-type-2Test(fe43e022-1664-426e-aaa0-eeffafb38226).html

المؤلفون: Warren, C, James, Louise A, Ramsden, Richard T, Wallace, A, Baser, Michael E, Varley, Jennifer, Evans, D Gareth R

المساهمون: Cancer Research UK Department of Cancer Genetics, The Paterson Institute for Cancer Research, Manchester, UK.

مصطلحات موضوعية: Adolescent, Adult, Aged, Child, Chromosome Aberrations, Chromosome Deletion, Chromosomes, Human, Pair 9, Female, Gene Amplification, Genes, Neurofibromatosis 2, Humans, Loss of Heterozygosity, Male, Middle Aged, Neuroma, Acoustic, Nucleic Acid Hybridization, Recurrence

العلاقة: Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation. 2003, 40 (11):802-6 J. Med. Genet.; http://hdl.handle.net/10541/81285Test; Journal of Medical Genetics

الإتاحة: https://doi.org/10.1136/jmg.40.11.802Test
http://hdl.handle.net/10541/81285Test

المؤلفون: Varley, Jennifer, Thorncroft, Mary R, McGown, Gail, Appleby, J, Kelsey, Anna M, Tricker, K J, Evans, D Gareth R, Birch, Jillian M

المساهمون: CRC Department of Cancer Genetics, Paterson Institute for Cancer Research, Manchester, UK.

مصطلحات موضوعية: Cancer, Chromosome Deletion, Chromosomes, Human, Pair 17, Genes, p53, Humans, Li-Fraumeni Syndrome, Mutation, Neoplasms

العلاقة: A detailed study of loss of heterozygosity on chromosome 17 in tumours from Li-Fraumeni patients carrying a mutation to the TP53 gene. 1997, 14 (7):865-71 Oncogene; 9047394; http://hdl.handle.net/10541/95215Test; Oncogene

الإتاحة: https://doi.org/10.1038/sj.onc.1201041Test
http://hdl.handle.net/10541/95215Test

المؤلفون: Hoban, Paul R, Cowen, Rachel L, Mitchell, Erika L D, Evans, D Gareth R, Kelly, M, Howard, P J, Heighway, Jim

المساهمون: CRC Department of Cancer Genetics, Paterson Institute for Cancer Research, Christie Hospital (NHS) Trust, Manchester, UK.

مصطلحات موضوعية: Wilms Tumour, Chromosome Fragility, Chromosome Mapping, Chromosomes, Human, Pair 5, Pair 6, Heterozygote, Humans, In Situ Hybridization, Fluorescence, Infant, Male, Translocation, Genetic, Wilms Tumor

العلاقة: Physical localisation of the breakpoints of a constitutional translocation t(5;6)(q21;q21) in a child with bilateral Wilms' tumour. 1997, 34 (4):343-5 J. Med. Genet.; 9138163; http://hdl.handle.net/10541/95488Test; Journal of Medical Genetics

الإتاحة: https://doi.org/10.1136/jmg.34.4.343Test
http://hdl.handle.net/10541/95488Test

المؤلفون: Cowan, Richard A, Hoban, Paul R, Kelsey, Anna M, Birch, Jillian M, Gattamaneni, Rao, Evans, D Gareth R

المساهمون: CRC Department of Cancer Genetics, Christie Hospital, Manchester, UK.

مصطلحات موضوعية: Cerebellar Cancer, Tumour Suppressor Genes, Basal Cell Nevus Syndrome, Cerebellar Neoplasms, Child, Preschool, Chromosomes, Human, Pair 9, Female, Genes, Tumor Suppressor, Heterozygote, Humans, Infant, Linkage (Genetics), Male, Medulloblastoma, Microsatellite Repeats, Pedigree

العلاقة: The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma. 1997, 76 (2):141-5 Br. J. Cancer; 9231911; http://hdl.handle.net/10541/94736Test; British Journal of Cancer

الإتاحة: http://hdl.handle.net/10541/94736Test

المؤلفون: Gokhale, D A, Evans, D Gareth R, Crowther, Derek, Woll, Penella J, Watson, C J, Dearden, S P, Fergusson, W D, Stevens, R F, Taylor, G M

المساهمون: Department of Medical Genetics, St Marys Hospital, Manchester, UK.

مصطلحات موضوعية: Adolescent, Adult, Base Sequence, Chromosomes, Human, Pair 2, Pair 8, Family Health, Female, HLA-DP Antigens, Histocompatibility Antigens Class I, Histocompatibility Antigens Class II, Histocompatibility Testing, Hodgkin Disease, Humans, Linkage (Genetics), Male, Middle Aged, Molecular Sequence Data, Mutation, Osteochondrodysplasias, Pedigree, Risk Factors

العلاقة: Molecular genetic analysis of a family with a history of Hodgkin's disease and dyschondrosteosis. 1995, 9 (5):826-33 Leukemia; 7769845; http://hdl.handle.net/10541/99250Test; Leukemia

الإتاحة: http://hdl.handle.net/10541/99250Test

المؤلفون: Teare, M Dawn, Santibanez-Koref, Mauro F, Wallace, S A, White, Gavin R M, Evans, D Gareth R, Burnell, Liza D, Harris, Martin, Howell, Anthony, Birch, Jillian M

المساهمون: Cancer Research Campaign Pediatric and Familial Cancer Research Group, Christie Hospital, Manchester, England.

مصطلحات موضوعية: Breast Cancer, Hereditary Cancerous Syndromes, Adult, Aged, Breast Neoplasms, Chromosome Mapping, Chromosomes, Human, Pair 17, Family Health, Female, Genetic Markers, Humans, Linkage (Genetics), Lod Score, Male, Middle Aged, Neoplastic Syndromes, Hereditary, Pedigree, Proto-Oncogenes

العلاقة: A linkage study in seven breast cancer families. 1993, 52 (4):786-8 Am. J. Hum. Genet.; 8460644; http://hdl.handle.net/10541/100068Test; American Journal of Human Genetics

الإتاحة: http://hdl.handle.net/10541/100068Test