المؤلفون: C. J. Hess, N. Ameziane, G. J. Schuurhuis, A. Errami, F. Denkers, G. J. L. Kaspers, J. Cloos, H. Joenje, D. Reinhardt, G. J. Ossenkoppele, C. M. Zwaan, Q. Waisfisz

المصدر: Cellular Oncology, Vol 30, Iss 4, Pp 299-306 (2008)

مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Cytology, QH573-671

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1570-5870Test; https://doaj.org/toc/1875-8606Test

الوصول الحر: https://doaj.org/article/93ab040d3a0646af9e9ac38a739bc342Test

المؤلفون: A. Haitjema, B.W. Brandt, N. Ameziane, P. May, J. Heringa, J.P. de Winter, H. Joenje, J.C. Dorsman

المصدر: PLoS One (19326203) vol.8 (2013) nr.4 p.e62017

العلاقة: http://hdl.handle.net/11245/1.397800Test

الإتاحة: http://hdl.handle.net/11245/1.397800Test

المؤلفون: M.A.J.A. Hermsen, H. Joenje, F. Arwert, B.J.M. Braakhuis, J.P.A. Baak, A. Westerveld, R. Slater

المصدر: Oral Oncology (13688375) vol.33 (1997) p.414-418

العلاقة: http://hdl.handle.net/11245/1.137639Test

الإتاحة: http://hdl.handle.net/11245/1.137639Test

المؤلفون: H Joenje, Detlev Schindler, E. T. Korthof, Thomas Bettecken, Beatrice Schuster, Anneke B. Oostra, J.P. de Winter, Karolina Hain, A. W. M. Nieuwint, Chantal Stoepker, Yvonne Hilhorst-Hofstee, Katharina Eirich, Nicolaas G. J. Jaspers, Martin A. Rooimans, John Rouse, Jurgen Steltenpool

المساهمون: Human genetics, CCA - Oncogenesis, Molecular Genetics, Developmental Biology

المصدر: Nature Genetics, 43(2), 138-U85
Nature Genetics, 43(2), 138-141. Nature Publishing Group
Stoepker, C, Hain, K, Schuster, B, Hilhorst-Hofstee, Y, Rooimans, M A, Steltenpool, J, Oostra, A B, Eirich, K, Korthof, E T, Nieuwint, A W M, Jaspers, N G J, Bettecken, T, Joenje, H, Schindler, D, Rouse, J & de Winter, J P 2011, ' SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype ', Nature Genetics, vol. 43, no. 2, pp. 138-141 . https://doi.org/10.1038/ng.751Test
Nature Genetics, 43(2), 138-U85. Nature Publishing Group

مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Fanconi anemia, complementation group C, DNA repair, Regulator, nutritional and metabolic diseases, Interstrand crosslink, Biology, medicine.disease, chemistry.chemical_compound, Fanconi Anemia Proteins, chemistry, Genome maintenance, Fanconi anemia, hemic and lymphatic diseases, medicine, DNA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8467e540f6f3e29f23a5db1d26cf6e3Test
https://doi.org/10.1038/ng.751Test

المؤلفون: Juan A. Bueren, José A. Casado, Paula Río, Jesus Martinez, Helmut Hanenberg, Kerstin Göttsche, José C. Segovia, Ngan Ching Cheng, H Joenje, Fré Arwert, Henri J. van de Vrugt

المصدر: ResearcherID
Europe PubMed Central

مصطلحات موضوعية: Immunology, Stem cell factor, Cell Biology, Hematology, Biology, medicine.disease, Biochemistry, Molecular biology, FANCA, Haematopoiesis, medicine.anatomical_structure, Megakaryocyte, Fanconi anemia, Knockout mouse, medicine, Bone marrow, Progenitor cell

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b65dcf2043713142b0197e9740508856Test
https://doi.org/10.1182/blood.v100.6.2032Test

المؤلفون: H Joenje, Anneke B. Oostra, Fré Arwert, Małgorzata Z. Zdzienicka, Barbara C. Godthelp, Martin van der Valk, Ngan Ching Cheng, Mireille Koomen, Henri J. van de Vrugt

المصدر: Human Molecular Genetics. 11:273-281

مصطلحات موضوعية: Male, Mitomycin, Biology, Drug Hypersensitivity, Mice, Fanconi anemia, FANCG, Chromosome instability, Testis, Genetics, medicine, Animals, Fanconi Anemia Complementation Group G Protein, Molecular Biology, Genetics (clinical), Mice, Knockout, Chinese hamster ovary cell, Ovary, Mitomycin C, DNA, General Medicine, Fibroblasts, Hematopoietic Stem Cells, medicine.disease, Null allele, Molecular biology, FANCA, DNA-Binding Proteins, Fanconi Anemia, Infertility, Immunology, Female, Chromosome breakage, DNA Damage

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14df821979189e67254107fb8a641a37Test
https://doi.org/10.1093/hmg/11.3.273Test

المؤلفون: H Joenje, Stander Jansen, Rachel A. Gibson, Charmaine Havenga, Neil V. Morgan, Eliane Gluckman, Alex J. Tipping, Thomas Pearson, Christopher G. Mathew, L P Kuyt, T. De Ravel

المساهمون: Clinical sciences, Medical Genetics, Faculty of Medicine and Pharmacy

المصدر: Proceedings of the National Academy of Sciences. 98:5734-5739

مصطلحات موضوعية: Male, Molecular Sequence Data, Population, Biology, Polymorphism, Single Nucleotide, South Africa, Fanconi Anemia/genetics, Fanconi anemia, medicine, Humans, Allele, education, DNA Primers, Genetics, education.field_of_study, Multidisciplinary, Base Sequence, Genetic heterogeneity, Haplotype, Biological Sciences, medicine.disease, Founder Effect, FANCA, Pedigree, Fanconi Anemia, Haplotypes, Microsatellite, Female, mutation, Genealogy and Heraldry, Founder effect

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc91f87f7602e427f46a8594ca5f4f37Test
https://doi.org/10.1073/pnas.091402398Test

المؤلفون: H. Joenje, J. D. Beck, H.G. Doerr, E. Schoof

المصدر: Growth Hormone & IGF Research. 10:290-293

مصطلحات موضوعية: Male, Delayed puberty, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, Biology, Short stature, Nuclear Family, Growth hormone deficiency, Endocrinology, Fanconi anemia, Age Determination by Skeleton, Germany, Internal medicine, Genotype, medicine, Humans, Abnormalities, Multiple, Nuclear family, Growth Disorders, Netherlands, Puberty, Delayed, Human Growth Hormone, Genetic Complementation Test, Infant, Newborn, Infant, medicine.disease, Phenotype, Fanconi Anemia, Menarche, Female, medicine.symptom, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a9240e545fc138cbf2f4ba70502fcceTest
https://doi.org/10.1054/ghir.2000.0164Test

المؤلفون: GR Evans, H Joenje, Fré Arwert, Martin Digweed, Cigdem Altay, R. D. Wegner, Neil V. Morgan, André Reis, Kathrin Saar, Christopher G. Mathew, Quinten Waisfisz, J. de Winter, Peter A. J. Leegwater, Kenshi Komatsu, Jan C. Pronk

المساهمون: Clinical genetics, Clinical chemistry, Çocuk Sağlığı ve Hastalıkları

المصدر: American journal of human genetics, 64(5), 1400-1405. Cell Press
Waisfisz, Q, Altay, C, Leegwater, PA, de Winter, JP, Komatsu, K, Evans, GR, Wegner, RD, Reis, A, Joenje, H, Arwert, F, Mathew, CG, Pronk, JC, Saar, K, Morgan, NV & Digweed, M 1999, ' The Fanconi anemia group E gene, FANCE, maps to chromosome 6p ', American journal of human genetics, vol. 64, no. 5, pp. 1400-1405 . https://doi.org/10.1086/302385Test

مصطلحات موضوعية: Genetic Markers, Male, Fanconi anemia, complementation group C, Locus (genetics), Complementation analysis, Biology, FANCE, Gene mapping, Fanconi anemia, Homozygosity mapping, Genetics, medicine, Humans, Genetics(clinical), Cell fusion, Genetics (clinical), Genetics & Heredity, Genetic Complementation Test, Chromosome Mapping, Chromosome Fragility, medicine.disease, Genetic marker, FANCE Gene, Chromosomes, Human, Pair 6, Female, Chromosome 6p21-22, Research Article

وصف الملف: text/plain

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f761b278c59406b5bbb9a0956c6d725Test
https://hdl.handle.net/1871/20617Test

المؤلفون: A. Sobeck, S. Stone, B. deGraaf, J. deWinter, W. D. Wang, H. Joenje, J. Gautier, M. E. Hoatlin, COSTANZO, VINCENZO

المساهمون: A., Sobeck, S., Stone, B., Degraaf, Costanzo, Vincenzo, J., Dewinter, W. D., Wang, H., Joenje, J., Gautier, M. E., Hoatlin

وصف الملف: STAMPA

العلاقة: volume:104; firstpage:207A; lastpage:207A; numberofpages:1; journal:BLOOD; http://hdl.handle.net/11588/502386Test

الإتاحة: http://hdl.handle.net/11588/502386Test