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1Academic Journal
المؤلفون: Marc Ladanyi, Man Yee Lui, Cristina R Antonescu, Amber Krause-boehm, Alfons Meindl, Pedram Argani, John H Healey, Takafumi Ueda, Hideki Yoshikawa, Aurelia Meloni-ehrig, Poul Hb Sorensen, Fredrik Mertens, Nils M, Herman Van Den Berghe, Raf Sciot, Paola Dal Cin, Julia Bridge
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.476.1404; http://cureasps.org/library/1_Ladanyi_ASPS_01.pdf
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2Academic Journal
المساهمون: The Pennsylvania State University CiteSeerX Archives
المصدر: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/1d/3c/J_Cell_Biol_1996_Feb_1_132(3)_487-497.tar.gz
وصف الملف: application/zip
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3
المؤلفون: Herman Van den Berghe
المصدر: European Journal of Haematology. 43:47-51
مصطلحات موضوعية: Genetic Markers, Pathology, medicine.medical_specialty, Chromosomal translocation, Biology, Plasma cell, Small cell lymphoma, Translocation, Genetic, Leukemia, Plasma Cell, Biomarkers, Tumor, medicine, Chromosomes, Human, Humans, Small supernumerary marker chromosome, Multiple myeloma, Chromosome Aberrations, Genetics, Chromosome, Karyotype, Hematology, General Medicine, Aneuploidy, medicine.disease, Lymphoproliferative Disorders, Leukemia, medicine.anatomical_structure, Multiple Myeloma
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4
المؤلفون: Herman Van den Berghe
المصدر: Scandinavian Journal of Haematology. 36:78-81
مصطلحات موضوعية: 5q-syndrome, Pediatrics, medicine.medical_specialty, Preleukaemia, business.industry, Myelodysplastic syndromes, medicine, Hematology, Medical emergency, medicine.disease, business, Refractory anaemia
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5
المؤلفون: Françoise Meire, Herman Van den Berghe, Eric Legius, Koen Devriendt, Lieve Standaert, Jean-Pierre Fryns, E Baten
المصدر: Clinical Genetics. 49:237-241
مصطلحات موضوعية: medicine.medical_specialty, Pediatrics, Intellectual Disability, Internal medicine, Diseases in Twins, Genetics, medicine, Humans, Abnormalities, Multiple, Stigmata, Short philtrum, Child, Genetics (clinical), Psychomotor learning, Cohen syndrome, Progressive microcephaly, business.industry, medicine.disease, Hypotonia, VPS13B, Endocrinology, El Niño, Female, medicine.symptom, business, Follow-Up Studies
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6
المؤلفون: Herman Van den Berghe, Paul Petit, Jean-Pierre Fryns, J Schmit
المصدر: Clinical Genetics. 50:19-22
مصطلحات موضوعية: Adult, Heart Defects, Congenital, Male, Adolescent, Cleft Lip, Biology, Mice, Pregnancy, Intellectual Disability, Genetics, medicine, Animals, Humans, Abnormalities, Multiple, Eye Abnormalities, Child, Wolf–Hirschhorn syndrome, In Situ Hybridization, Fluorescence, Genetics (clinical), medicine.diagnostic_test, Hybridization probe, Infant, Newborn, Chromosome, Karyotype, Gene deletion, medicine.disease, Phenotype, Chromosome Banding, Cleft Palate, Child, Preschool, Karyotyping, Female, Chromosomes, Human, Pair 4, DNA Probes, Molecular probe, Gene Deletion, Fluorescence in situ hybridization
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7
المؤلفون: Myriam Welkenhuysen, Gerry Evers-Kiebooms, Jean-Jacques Cassiman, Lieve Denayer, Herman Van den Berghe
المصدر: Clinical Genetics. 46:336-343
مصطلحات موضوعية: Adult, Male, Heterozygote, Adolescent, Cystic Fibrosis, media_common.quotation_subject, Cystic fibrosis, Heterozygote Detection, Surveys and Questionnaires, Genetics, medicine, Humans, Genetics (clinical), Aged, media_common, Social adaptation, Gene carrier, Genetic Carrier Screening, Middle Aged, medicine.disease, Cognitive bias, Feeling, Illusory superiority, Carrier status, Female, Psychology, Prejudice, Clinical psychology
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8
المؤلفون: Lieve Denayer, Herman Van den Berghe, Gerry Evers-Kiebooms
المصدر: Clinical Genetics. 37:207-215
مصطلحات موضوعية: Adult, Male, Parents, Risk, Health Knowledge, Attitudes, Practice, medicine.medical_specialty, Firstborn, Cystic Fibrosis, Psychometrics, Offspring, Genetic counseling, Decision Making, Genetic Counseling, Prenatal diagnosis, Belgium, Pregnancy, Prenatal Diagnosis, Surveys and Questionnaires, Genetics, Humans, Medicine, Family, Child, Genetics (clinical), Fetus, business.industry, Obstetrics, medicine.disease, Contraception, Family planning, Family Planning Services, Regression Analysis, Female, Birth Order, business, Follow-Up Studies
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9
المؤلفون: Gerry Evers-Kiebooms, Lieve Denayer, Myriam Welkenhuysen, Herman Van den Berghe, Jean-Jacques Cassiman
المصدر: Clinical Genetics. 49:232-236
مصطلحات موضوعية: Adult, Heterozygote, Adolescent, Cystic Fibrosis, Psychometrics, business.industry, Genetic counseling, Self-concept, Anxiety, Self Concept, Test (assessment), Interviews as Topic, Multivariate analysis of variance, Surveys and Questionnaires, Genetics, medicine, Humans, Psychological testing, Analysis of variance, medicine.symptom, business, Genetics (clinical), Clinical psychology
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10
المؤلفون: Krystyna H. Chrzanowska, Herman Van den Berghe, J. P. Fryns, Małgorzata Krajewska-Walasek, L. Wisniewski
المصدر: Clinical Genetics. 35:157-160
مصطلحات موضوعية: Male, behavioral disciplines and activities, Facial Bones, Lower limb, Fingers, Genetics, medicine, Humans, Abnormalities, Multiple, Nager Acrofacial Dysostosis Syndrome, Craniofacial, Child, Genetics (clinical), business.industry, Dysostoses, Infant, Dysostosis, Syndrome, Anatomy, Toes, medicine.disease, Phenotype, Miller syndrome, Female, business
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11
المؤلفون: Paul Petit, J. P. Fryns, Herman Van den Berghe, J. Koumans
المصدر: Clinical Genetics. 21:384-387
مصطلحات موضوعية: DNA Replication, endocrine system, congenital, hereditary, and neonatal diseases and abnormalities, X Chromosome, Adolescent, Kinetics, Turner Syndrome, Biology, Long arm, Short stature, mental disorders, Turner syndrome, Genetics, medicine, Humans, Genetics (clinical), X chromosome, Chromosome Aberrations, Sex Chromosomes, Karyotype, medicine.disease, Chromosome Banding, nervous system diseases, Female, medicine.symptom
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12
المؤلفون: Jean-Pierre Fryns, Koenraad Devriendt, Herman Van den Berghe
المصدر: Clinical Genetics. 49:6-9
مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, business.industry, Hypogonadism, Alopecia, medicine.disease, Central nervous system disease, Epilepsy, Endocrinology, Hypergonadotropic hypogonadism, Seizures, Congenital total alopecia, Intellectual Disability, Internal medicine, Genetics, Childhood convulsions, Humans, Medicine, business, Genetics (clinical)
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13
المصدر: Clinical Genetics. 29:191-195
مصطلحات موضوعية: Male, Biology, Meiosis, Fragile X chromosome, Intellectual Disability, Diseases in Twins, Genetics, medicine, Humans, Lymphocytes, Allele, Alleles, Cells, Cultured, Sex Chromosome Aberrations, Genetics (clinical), X chromosome, Chromosomal fragile site, Genetic Variation, Chromosome Fragility, Heritability, medicine.disease, Fragile X syndrome, Fragile X Syndrome, Female
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14
المؤلفون: Jo Van Dorpe, Herman Van den Berghe, Fred Van Leuven, Raphael Sciot, Paola Dal Cin, Christopher D.M. Fletcher, Ivo De Wever, Stanislawa Weremowicz
المصدر: Virchows Archiv. 440:485-490
مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, Biopsy, Chromosomal translocation, Biology, Translocation, Genetic, Desmin, Pathology and Forensic Medicine, Benign tumor, Mesenchymoma, Benign Mesenchymoma, medicine, Humans, Molecular Biology, In Situ Hybridization, Fluorescence, Chromosomes, Human, Pair 15, Muscle Neoplasms, Chromosomes, Human, Pair 12, medicine.diagnostic_test, HMGA2 Protein, S100 Proteins, Cytogenetics, Cell Biology, General Medicine, Gene rearrangement, Middle Aged, medicine.disease, Immunohistochemistry, Actins, Karyotyping, Chromosome abnormality, Fluorescence in situ hybridization
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15
المؤلفون: Raphael Sciot, Christopher D.M. Fletcher, Roberta Vanni, Nils Mandahl, Helena Willén, Juan Rosai, Peter Brys, Fredrik Mertens, Howard D. Dorfman, Herman Van den Berghe, Anders Rydholm, Kjell Jonson, Ignace Samson, Felix Mitelman, Paola Dal Cin, Giovanni Tallini, Ivo De Wever
المصدر: The Journal of Pathology. 196:194-203
مصطلحات موضوعية: musculoskeletal diseases, Osteochondroma, Pathology, medicine.medical_specialty, Chondromyxoid fibroma, Chondroblastoma, Biology, medicine.disease, Myxoid chondrosarcoma, Pathology and Forensic Medicine, medicine, Sarcoma, Chondrosarcoma, Fibroma, Chondroma
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16
المؤلفون: A. Lee Soreng, Jonathan A. Fletcher, Marisa R. Nucci, Patrick Pauwels, Frank C. Kuo, Paola Dal Cin, Herman Van den Berghe, Jeffrey Sklar, Jason I. Koontz
المصدر: Proceedings of the National Academy of Sciences. 98:6348-6353
مصطلحات موضوعية: Chromosomes, Artificial, Bacterial, Stromal cell, Sarcoma, Endometrial Stromal, Molecular Sequence Data, Classification scheme, Biology, Translocation, Genetic, Humans, Amino Acid Sequence, Chromosomes, Artificial, Yeast, Gene, YWHAE, Chromosome 7 (human), Genetics, Multidisciplinary, Base Sequence, Breakpoint, DNA, Neoplasm, Middle Aged, Biological Sciences, Artificial Gene Fusion, Endometrial Neoplasms, Neoplasm Proteins, DNA-Binding Proteins, Blotting, Southern, Endometrial stromal nodule, Cancer research, Female, Endometrial stromal tumor, Co-Repressor Proteins, Chromosomes, Human, Pair 7, Chromosomes, Human, Pair 17, Transcription Factors
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17
المؤلفون: Herman Van den Berghe, Anders Rydholm, Giovanni Tallini, Felix Mitelman, Peter Brys, Christopher D.M. Fletcher, Fredrik Mertens, Howard D. Dorfman, Raf Sciot, Ignace Samson, Roberta Vanni, Nils Mandahl, Paola Dal Cin, Juan Rosai, Kjell Jonson, Ivo De Wever, Helena Willén
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Adolescent, Karyotypic abnormality, Bone Neoplasms, Chromosomal translocation, Biology, Pathology and Forensic Medicine, medicine, Humans, Giant Cell Tumors, Chromosome Aberrations, Giant Cell Tumor of Bone, Chromosome, Karyotype, Aneurysmal bone cyst, Anatomy, Middle Aged, medicine.disease, Bone Cysts, Aneurysmal, Giant cell, Karyotyping, Female, Chromosomes, Human, Pair 16, Chromosomes, Human, Pair 17, Giant-cell tumor of bone
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18
المؤلفون: Christopher D.M. Fletcher, Helena Willén, Herman Van den Berghe, Raphael Sciot, Anders Rydholm, Felix Mitelman, Nils Mandahl, Roberta Vanni, Ivo De Wever, Fredrik Mertens, Paola Dal Cin, Giovanni Tallini, Juan Rosai
المصدر: Modern Pathology. 13:1080-1085
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Soft Tissue Neoplasm, Fibromatosis, medicine, Karyotype, Biology, Fibroma, medicine.disease, Trisomy, Pathology and Forensic Medicine
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19
المؤلفون: K Hinz, Anne Hagemeijer, Herman Van den Berghe, Lucienne Michaux, Judith Dierlamm, Dieter K. Hossfeld, M Stefanova, Iwona Wlodarska
المصدر: Hematological Oncology. 18:1-13
مصطلحات موضوعية: Cancer Research, Pathology, medicine.medical_specialty, Lymphoma, B-Cell, Biology, Inhibitor of apoptosis, Proto-Oncogene Mas, Translocation, Genetic, immune system diseases, hemic and lymphatic diseases, medicine, Humans, Chromosome Aberrations, Chromosomes, Human, Pair 14, Chromosomes, Human, Pair 11, Large cell, MALT lymphoma, Lymphoma, B-Cell, Marginal Zone, Hematology, General Medicine, Marginal zone, medicine.disease, BCL6, BCL10, Lymphoma, Oncology, Chromosomes, Human, Pair 1, Mutation, Cancer research, Marginal zone B-cell lymphoma, Chromosomes, Human, Pair 18
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7897f06e15f0afbff63814ece950d38
https://doi.org/10.1002/(sici)1099-1069(200003)18:1<1::aid-hon647>3.0.co;2-g -
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المؤلفون: Fredrik Mertens, Nils Mandahl, Giovanni Tallini, Ivo De Wever, Herman Van den Berghe, Paola Dal Cin, R. Vanni, Christopher D.M. Fletcher, Anders Rydholm, Helena Willén, Raf Sciot, Juan Rosai, Felix Mitelman
المصدر: Cancer Genetics and Cytogenetics. 116:66-73
مصطلحات موضوعية: Leiomyosarcoma, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, medicine.medical_specialty, Pathology, Breakpoint, Cytogenetics, Soft tissue, Karyotype, Anatomy, Biology, medicine.disease, Genetics, medicine, Histopathology, Spindle cell sarcoma, Chromosome breakage, Molecular Biology