المؤلفون: Elkjaer Andersen, Rikke, Sauer Mikkelsen, Carsten, Bygum, Anette

المصدر: Månedsskrift for Almen Praksis. 94(12):908

المؤلفون: Wahlgren, Carl-Fredrik

المصدر: Barnläkaren. 9(2):20

المؤلفون: Brandell, R R

المصدر: Medicinsk Access. 5(8-9):52

المؤلفون: Nimeus, E, Annertz, K, Fernö, M, Rennstam, K, Åkervall, J, Wennerberg, J

المصدر: Svensk ÖNH-tidskrift. 8(1):24

المؤلفون: Stefania Gimelli, Stylianos E. Antonarakis, Maria Teresa Divizia, Frédérique Béna, Lara Bricco, Giorgio Gimelli, Roberto Ravazzolo, Margherita Lerone

المصدر: American Journal of Medical Genetics. A, Vol. 152A, No 8 (2010) pp. 2130-2133

مصطلحات موضوعية: Male, Translocation, Genetic/*genetics, WAGR Syndrome/*genetics, WAGR syndrome, Chromosomal translocation, Biology, Translocation, Genetic, Fathers, WAGR Syndrome, Chromosomes, Human, Pair 2/*genetics, Genetics, medicine, Comparative Genomic Hybridization, Humans, ddc:576.5, In Situ Hybridization, Fluorescence, Genetics (clinical), Oligonucleotide Array Sequence Analysis, Chromosomes, Human, Pair 11, Infant, Newborn, medicine.disease, Chromosomes, Human, Pair 2, Chromosomes, Human, Pair 11/*genetics

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af01437bbf7941b7297128daf4453082Test
https://doi.org/10.1002/ajmg.a.33517Test

المؤلفون: Marie-Magdeleine Ruchoux, Jacqueline Mikol, Isabelle Salmon, Dominique Figarella-Branger, David W. Ellison, Emmanuel Rousseau, Francesco Scaravilli, Catherine Lacroix, Thomas Palm, Catherine Godfraind, Miikka Vikkula, Françoise Chapon

المساهمون: UCL - MD/MNOP - Département de morphologie normale et pathologique, UCL - MD/BICL - Département de biochimie et de biologie cellulaire, UCL - (SLuc) Service d'anatomie pathologique, UCL - (SLuc) Centre de génétique médicale UCL, UCL - (SLuc) Centre de malformations vasculaires congénitales

المصدر: Molecular Cancer, Vol 6, Iss 1, p 47 (2007)
Molecular Cancer, Vol. 6, p. 47 [1-10] (2007)
Molecular Cancer
Molecular cancer, 6

مصطلحات موضوعية: Ependymoma, Chromosomes, Human, Pair 11 -- genetics, Microsatellite Repeats -- genetics, Male, Pathology, Cancer Research, Tissue Fixation, Trisomy, medicine.disease_cause, Chromosomes, Human, Pair 19 -- genetics, Child, Glial fibrillary acidic protein, biology, Brain Neoplasms, Nucleic Acid Hybridization, Sciences bio-médicales et agricoles, Middle Aged, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Oncology, Child, Preschool, Molecular Medicine, Female, Chromosome Deletion, Ependymoma -- pathology, Chromosomes, Human, Pair 9, Adult, medicine.medical_specialty, Adolescent, Chromosome 9, Brain Neoplasms -- genetics, Polymorphism, Single Nucleotide, lcsh:RC254-282, Brain Neoplasms -- pathology, Chromosome 19, medicine, Humans, Tissue Array Analysis -- methods, Ependymoma -- genetics, Aged, Genome, Human, Research, Chromosomes, Human, Pair 11, Infant, Tissue Fixation -- methods, medicine.disease, Nucleic Acid Hybridization -- methods, Tissue Array Analysis, biology.protein, Human genome, Carcinogenesis, Chromosomes, Human, Pair 9 -- genetics, Chromosomes, Human, Pair 19, Clear cell, Microsatellite Repeats

وصف الملف: 1 full-text file(s): application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0af54cbe2d2dac6f2f69f1a8c767f0baTest
http://www.molecular-cancer.com/content/6/1/47Test

المؤلفون: K L Tsun, Ui-Soon Khoo, H Y S Ngan, B S Y Leung, P M Chiu, Annie N.Y. Cheung

المصدر: Journal of clinical pathology. 57(7)

مصطلحات موضوعية: Telomerase, Pathology, medicine.medical_specialty, Uterine Cervical Neoplasms, Uterine cervical neoplasms - diagnosis - genetics, Context (language use), Cervical intraepithelial neoplasia, Pathology and Forensic Medicine, Immunoenzyme Techniques, Chromosomes, human, pair 11 - genetics, Chromosomes, human, pair 16 - genetics, Cytology, medicine, Carcinoma, Biomarkers, Tumor, Humans, CISH, In Situ Hybridization, Vaginal Smears, biology, Chromosomes, Human, Pair 11, General Medicine, Original Articles, medicine.disease, Uterine Cervical Dysplasia, Molecular biology, Koilocyte, Ki-67 Antigen, Ki-67, biology.protein, Carcinoma, Squamous Cell, Female, Tumor markers, biological - metabolism, In situ hybridization - methods, Chromosomes, Human, Pair 16

وصف الملف: 196203 bytes; 3013 bytes; application/pdf; text/plain

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37b64eb102dc26e27fb599fa1dd608eaTest
https://pubmed.ncbi.nlm.nih.gov/15220365Test

المؤلفون: Syrrou, M., Fryns, J. P.

مصطلحات موضوعية: Male, Models, Genetic, Infant, Chromosome Deletion, Chromosome Banding, Developmental Disabilities/*genetics, Phenotype, Child, Preschool, Chromosomes, Human, Pair 11/*genetics, Karyotyping, Humans, Chromosome Fragility/genetics, Female, In Situ Hybridization, Fluorescence, Psychomotor Performance

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_____10561::6a07313e343b29abe671c867ed283b1bTest
http://olympias.lib.uoi.gr/jspui/handle/123456789/20688Test

المصدر: Annals of hematology, 95 (1

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adolescent, Child, Child, Preschool, Chromosomes, Human, Pair 11 -- genetics, Chromosomes, Human, Pair 14 -- genetics, Cohort Studies, Female, Humans, Male, Precursor T-Cell Lymphoblastic Leukemia-Lymphoma -- diagnosis -- genetics -- mortality, Prospective Studies, Retrospective Studies, Survival Rate -- trends, Translocation, Genetic -- genetics, Treatment Outcome, Pediatric acute lymphoblastic leukemia, Prognosis, T cell, Translocation t(11;14), info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/264799Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest

المصدر: Molecular cancer, 6

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adolescent, Adult, Aged, Brain Neoplasms -- genetics, Brain Neoplasms -- pathology, Child, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 11 -- genetics, Chromosomes, Human, Pair 19 -- genetics, Chromosomes, Human, Pair 9 -- genetics, Ependymoma -- genetics, Ependymoma -- pathology, Female, Genome, Human, Humans, Infant, Male, Microsatellite Repeats -- genetics, Middle Aged, Nucleic Acid Hybridization -- methods, Polymorphism, Single Nucleotide, Tissue Array Analysis -- methods, Tissue Fixation -- methods, Trisomy, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: https://dipot.ulb.ac.be/dspace/bitstream/2013/53616/4/doi_28946.pdfTest
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/53616Test
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLLTest