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1دورية أكاديمية
المؤلفون: Imke M. Veltman, Joris A. Veltman, Ger Arkesteijn, Irene M. Janssen, Lisenka E. Vissers, Pieter J. de Jong, Ad Geurts van Kessel, Eric F.P.M. Schoenmakers
المصدر: BioTechniques, Vol 35, Iss 5, Pp 1066-1070 (2003)
مصطلحات موضوعية: Biology (General), QH301-705.5
العلاقة: https://doaj.org/toc/0736-6205Test; https://doaj.org/toc/1940-9818Test; https://doaj.org/article/1db7e87d00a74ad48b6e523a9ee24e1dTest
الإتاحة: https://doi.org/10.2144/03355dd03Test
https://doaj.org/article/1db7e87d00a74ad48b6e523a9ee24e1dTest -
2
المؤلفون: Erik Huys, Patrick Pauwels, Marga Schepens, Maria Debiec-Rychter, B. P. M. Janssen, Eric F.P.M. Schoenmakers, Ad Geurts van Kessel, Gerard Merkx, Lianne Hermers, M. A. S. H. Kersten, Jens Bunt
المصدر: Genes, Chromosomes & Cancer, 52, 11-23
Genes, Chromosomes & Cancer, 52, 1, pp. 11-23مصطلحات موضوعية: Cancer Research, Pathology, medicine.medical_specialty, Positional cloning, Molecular Sequence Data, Biology, Genomic disorders and inherited multi-system disorders [IGMD 3], HMGA2, Biomarkers, Tumor, Genetics, medicine, Humans, Amino Acid Sequence, Genetics and epigenetic pathways of disease Translational research [NCMLS 6], Uterine Neoplasm, In Situ Hybridization, Fluorescence, Chromosomal inversion, Homeodomain Proteins, Uterine leiomyoma, Base Sequence, Leiomyoma, Pelvic pain, Nuclear Proteins, Chromosome, Middle Aged, medicine.disease, Repressor Proteins, Uterine Neoplasms, biology.protein, Female, medicine.symptom, Chromosomes, Human, Pair 7, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fab29a84f1981d00dfd7d351e220698eTest
https://doi.org/10.1002/gcc.22001Test -
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المؤلفون: Merel A.W. Oortveld, Ellen A.W. Blokland, Frans P.M. Cremers, Erik Huys, Jyoti Agrawal, C. Erik van Nouhuys, Dominique Smeets, Eric F.P.M. Schoenmakers, Dorien Lugtenberg, Annette Schenck, Gerard Merkx, Jamie M. Kramer, Arijit Mukhopadhyay, Ad Geurts van Kessel, Hans van Bokhoven
المصدر: Human Genetics
Human Genetics, 128, 281-91
Human Genetics, 128, 3, pp. 281-91مصطلحات موضوعية: Adult, Microcephaly, Pathology, medicine.medical_specialty, Genetics and epigenetic pathways of disease [NCMLS 6], Biology, Retina, Genomic disorders and inherited multi-system disorders [IGMD 3], Species Specificity, Intellectual Disability, Genetics, medicine, Animals, Drosophila Proteins, Humans, Genetics(clinical), Abnormalities, Multiple, In Situ Hybridization, Fluorescence, Genetics (clinical), DNA Primers, Original Investigation, Chromosomal inversion, Base Sequence, medicine.diagnostic_test, Genetic heterogeneity, Breakpoint, Cyclin-Dependent Kinase 8, medicine.disease, Cyclin-Dependent Kinases, Karyotyping, Chromosome Inversion, Eye development, Chromosomes, Human, Pair 6, Drosophila, Female, Falciform retinal fold, Haploinsufficiency, Functional Neurogenomics [DCN 2], Fluorescence in situ hybridization
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e261eabaee4e65e7945e7f215b3b08cTest
https://doi.org/10.1007/s00439-010-0848-xTest -
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المؤلفون: Lutgarde Govaerts, Nicoline Hoogerbrugge, Eugène T P Verwiel, Eveline J. Kamping, Eric F.P.M. Schoenmakers, Roland P. Kuiper, Evelyne Lerut, Lilian Vreede, Eamonn R. Maher, Femke van Erp, Anita Bonne, Lianne van Kempen, Maria Debiec-Rychter, Ad Geurts van Kessel, Ramprasath Venkatachalam, Chris Ricketts
المساهمون: Pathology, Clinical Genetics, Medical Oncology, Internal Medicine
المصدر: Cancer Genetics and Cytogenetics, 195, 105-11
Cancer Genetics and Cytogenetics, 195, 2, pp. 105-11
Cancer Genetics & Cytogenetics, 195(2), 105-111. Elsevier Inc.مصطلحات موضوعية: Cancer Research, F-Box-WD Repeat-Containing Protein 7, Genetics and epigenetic pathways of disease [NCMLS 6], Derivative chromosome, Tumor suppressor gene, Ubiquitin-Protein Ligases, Cell Cycle Proteins, Single-nucleotide polymorphism, Biology, medicine.disease_cause, Polymerase Chain Reaction, Translocation, Genetic, Molecular epidemiology [NCEBP 1], SDG 3 - Good Health and Well-being, Translational research [ONCOL 3], Chromosome instability, Genetics, medicine, Humans, Cell division control protein 4, Carcinoma, Renal Cell, Molecular Biology, Gene, In Situ Hybridization, Fluorescence, DNA Primers, Mutation, Base Sequence, Hereditary cancer and cancer-related syndromes [ONCOL 1], FBXW7 Gene, F-Box Proteins, Kidney Neoplasms, Karyotyping, Chromosomes, Human, Pair 3, Chromosomes, Human, Pair 4
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e98f3ec8943b248306adbd06dd28d3c4Test
https://doi.org/10.1016/j.cancergencyto.2009.07.001Test -
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المؤلفون: Donatella Milani, Paola Castronovo, Gaia Roversi, Maura Masciadri, Rolph Pfundt, Eric F.P.M. Schoenmakers, Lidia Larizza, Giuseppe Zampino, Silvia Russo, Angelo Selicorni, Cristina Gervasini
المساهمون: Gervasini, C, Pfundt, R, Castronovo, P, Russo, S, Roversi, G, Masciadri, M, Milani, D, Zampino, G, Selicorni, A, Schoenmakers, E, Larizza, L
المصدر: Clinical Genetics, 74, 6, pp. 531-8
Clinical Genetics, 74, 531-8مصطلحات موضوعية: Male, Cornelia de Lange Syndrome, Genetics and epigenetic pathways of disease [NCMLS 6], Chromosomal Proteins, Non-Histone, Cell Cycle Proteins, Biology, medicine.disease_cause, De Lange Syndrome, Cell Cycle Protein, Gene duplication, Genetics, medicine, Humans, Copy-number variation, Genetics (clinical), Molecular diagnosis, prognosis and monitoring [UMCN 1.2], Mutation, Comparative Genomic Hybridization, Genome, Human, Protein, Proteins, NIPBL, CORNELIA DE LANGE, medicine.disease, Phenotype, Human genetics, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, Female, Chromosome Deletion, Comparative genomic hybridization
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c90163583fe8783a52fe9597fe91349bTest
https://hdl.handle.net/2066/71071Test -
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المؤلفون: Andrew C. Lidral, Kazutoyo Osoegawa, Maria A. Mansilla, Kagistia Hana Utami, W. A. van der Vliet, Eric F.P.M. Schoenmakers, Åke Borg, Jeffrey C. Murray, P. J. De Jong, Marla K. Johnson, Edward J. Lammer, G. M. Vessere, Brian C. Schutte, Rolph Pfundt, Johan Staaf, Bridget M. Riley, Jamie L'Heureux
المصدر: Journal of Medical Genetics, 45, 81-6
Journal of Medical Genetics, 45, 2, pp. 81-6مصطلحات موضوعية: Male, Chromosomes, Artificial, Bacterial, Candidate gene, Genetics and epigenetic pathways of disease [NCMLS 6], Chromosomes, Human, Pair 22, Cleft Lip, Gene Dosage, Biology, Gene dosage, Article, Gene mapping, DiGeorge syndrome, Genetics, medicine, Humans, Van der Woude syndrome, Child, Gene, Genetics (clinical), Base Sequence, Chromosomes, Human, Pair 10, Chromosome Mapping, Genetic Variation, Nucleic Acid Hybridization, Chromosome, DNA, Syndrome, medicine.disease, Cleft Palate, Phenotype, Chromosomes, Human, Pair 6, Female, IRF6, Chromosome Deletion, Immunity, infection and tissue repair [NCMLS 1]
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb45c7bc3b8e9e633d8c3bf443fafc24Test
https://doi.org/10.1136/jmg.2007.052191Test -
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المؤلفون: Jayne Y. Hehir-Kwa, Peter M. Hoogerbrugge, Eric F.P.M. Schoenmakers, S.V. van Reijmersdal, Roland P. Kuiper, F.N. van Leeuwen, A. Geurts van Kessel
المصدر: Leukemia, 21, 1258-66
Leukemia, 21, 6, pp. 1258-66مصطلحات موضوعية: Male, Cancer Research, Age-related aspects of cancer [ONCOL 2], Genetics and epigenetic pathways of disease [NCMLS 6], Cellular differentiation, Gene Dosage, Biology, medicine.disease_cause, Recombination-activating gene, Immune Regulation [NCMLS 2], Translational research [ONCOL 3], CDKN2A, hemic and lymphatic diseases, medicine, Humans, Lymphocytes, Molecular diagnosis, prognosis and monitoring [UMCN 1.2], Chromosome Aberrations, Genetics, B-Lymphocytes, Hereditary cancer and cancer-related syndromes [ONCOL 1], Gene Expression Profiling, Cell Cycle, Lymphocyte differentiation, Nucleic Acid Hybridization, Cell Differentiation, Immunotherapy, gene therapy and transplantation [UMCN 1.4], Genomics, Hematology, Precursor Cell Lymphoblastic Leukemia-Lymphoma, ETV6, Oncology, Female, CDKN1B, Carcinogenesis, BTG1, Genes, Neoplasm, Transcription Factors
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d9bccd3da50d83244d7e51f16d9d87Test
https://doi.org/10.1038/sj.leu.2404691Test -
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المؤلفون: Hans Stoop, J. Wolter Oosterhuis, Joris A. Veltman, Brenda Summersgill, H. Berna Beverloo, Ad J. M. Gillis, Rolph Pfundt, Ellen van Drunen, Alan McIntyre, Ruud J.H.L.M. van Gurp, Peter J. van der Spek, Ad Geurts van Kessel, Remko Hersmus, Renee Reijo Pera, Eric F.P.M. Schoenmakers, Leendert H. J. Looijenga, Janet Shipley, Dominik T. Schneider
المساهمون: Pathology, Clinical Genetics, Molecular Genetics
المصدر: Cancer Research, 66(1), 290-302. American Association for Cancer Research Inc.
Cancer Research, 66, 290-302
Cancer Research, 66, 1, pp. 290-302مصطلحات موضوعية: Male, Cancer Research, Candidate gene, Genetics and epigenetic pathways of disease [NCMLS 6], Chromosome 9, Spermatocyte, Biology, Genomic Instability, Testicular Neoplasms, Translational research [ONCOL 3], Spermatocytes, medicine, Biomarkers, Tumor, Humans, Molecular diagnosis, prognosis and monitoring [UMCN 1.2], Genetics, Ovarian Neoplasms, Hereditary cancer and cancer-related syndromes [ONCOL 1], Gene Expression Profiling, Chromosome, Seminoma, medicine.disease, Molecular biology, Immunohistochemistry, Gene expression profiling, medicine.anatomical_structure, Oncology, Spermatocytic seminoma, Female, Chromosomes, Human, Pair 9, Comparative genomic hybridization, Transcription Factors
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95e52aeefd704f0f79b093856caf014aTest
https://hdl.handle.net/2066/50081Test -
9
المؤلفون: Norma C. Gutiérrez, Jesús F. San Miguel, M. Jose Calasanz, Eric F.P.M. Schoenmakers, Francesc Solé, M. Belén González, Juan Luis García, Jesús M. Hernández
المصدر: Cancer Genetics and Cytogenetics. 150:136-143
مصطلحات موضوعية: Genetics, Chromosome 7 (human), Cancer Research, Myeloid, medicine.diagnostic_test, Breakpoint, Chromosomal translocation, Biology, medicine.disease, Pathogenesis, Myelogenous, Leukemia, medicine.anatomical_structure, medicine, Molecular Biology, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b78e7c862be97403c3b97e270bd69989Test
https://doi.org/10.1016/j.cancergencyto.2003.08.019Test -
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المؤلفون: Karin Leunen, Romaric Croes, Anne Hagemeijer, Eric F.P.M. Schoenmakers, Frédéric Amant, Maria Debiec-Rychter, Ignace Vergote
المساهمون: Academic Medical Center
المصدر: Gynecologic Oncology, 91, 1, pp. 265-71
Gynecologic oncology, 91(1), 265-271. Academic Press Inc.
Gynecologic Oncology, 91, 265-71مصطلحات موضوعية: Adult, medicine.medical_specialty, Sarcoma, Endometrial Stromal, medicine.medical_treatment, Translocation, Genetic, Diagnosis, Differential, Laparotomy, medicine, Humans, Molecular diagnosis, prognosis and monitoring [UMCN 1.2], Mesna, Gynecology, Chemotherapy, Endometrial stromal sarcoma, Ifosfamide, postpartum bleeding, Chromosomes, Human, Pair 10, business.industry, Postpartum Hemorrhage, Obstetrics and Gynecology, medicine.disease, Combined Modality Therapy, Endometrial Neoplasms, Oncology, Female, Sarcoma, Differential diagnosis, business, Chromosomes, Human, Pair 17, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb3738fd589d2ab3b2e9457fce1fc8e7Test
https://doi.org/10.1016/s0090-8258Test(03)00477-3