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1
المؤلفون: M, Rio, G, Royer, S, Gobin, M C, de Blois, C, Ozilou, A, Bernheim, M, Nizon, A, Munnich, J-P, Bonnefont, S, Romana, M, Vekemans, C, Turleau, V, Malan
المصدر: Clinical genetics. 84(1)
مصطلحات موضوعية: Recombination, Genetic, Comparative Genomic Hybridization, Genotype, Mosaicism, Developmental Disabilities, Membrane Proteins, Muscle Proteins, Nerve Tissue Proteins, Twins, Monozygotic, Phenotype, Child, Preschool, Chromosomes, Human, Pair 2, Karyotyping, Diseases in Twins, Humans, Female, Autistic Disorder, In Situ Hybridization, Fluorescence, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::33d43edacec93354a9d2138e2e8c0ec3Test
https://pubmed.ncbi.nlm.nih.gov/23061379Test -
2
المؤلفون: D, Sanlaville, J M, Lapierre, A, Coquin, C, Turleau, J, Vermeesch, L, Colleaux, G, Borck, M, Vekemans, A, Aurias, S P, Romana
المصدر: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 12(10)
مصطلحات موضوعية: Diagnosis, Differential, Karyotyping, Genetic Diseases, Inborn, Humans, Hybridization, Genetic, Genetic Testing, Child, Microarray Analysis
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::f59441d6f05343925b44a6a659f3a065Test
https://pubmed.ncbi.nlm.nih.gov/16153813Test -
3
المؤلفون: H K, Benailly, J M, Lapierre, B, Laudier, J, Amiel, T, Attié, M C, De Blois, M, Vekemans, S P, Romana
المصدر: Clinical genetics. 64(3)
مصطلحات موضوعية: Homeodomain Proteins, Developmental Disabilities, Limb Deformities, Congenital, Infant, Nucleic Acid Hybridization, Enteric Nervous System, Translocation, Genetic, Face, Karyotyping, Aborted Fetus, Humans, Abnormalities, Multiple, Female, Hirschsprung Disease, RNA, Messenger, Chromosomes, Human, Pair 4, Facial Neoplasms, Hemangioma, Gene Deletion, In Situ Hybridization, Chromosomes, Human, Pair 8, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::f7d8e289fd758e82cae81f07c5fd1427Test
https://pubmed.ncbi.nlm.nih.gov/12919134Test -
4
المؤلفون: D, Sanlaville, S P, Romana, J M, Lapierre, J, Amiel, D, Genevieve, C, Ozilou, M, Le Lorch, S, Brisset, P, Gosset, C, Baumann, C, Turleau, S, Lyonnet, M, Vekemans
المصدر: Clinical genetics. 61(2)
مصطلحات موضوعية: Chromosome Aberrations, Heart Defects, Congenital, Male, Homozygote, Nucleic Acid Hybridization, Ear, Syndrome, Choanal Atresia, Chromosomes, Cohort Studies, Coloboma, Karyotyping, Humans, Abnormalities, Multiple, Female, Genitalia, Growth Disorders, In Situ Hybridization, Fluorescence
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::d491f501e2839603d6b54ee1b1c95eeeTest
https://pubmed.ncbi.nlm.nih.gov/11940088Test -
5
المؤلفون: D, Mahieu-Caputo, M V, Senat, S, Romana, V, Houfflin-Debarge, P, Gosset, F, Audibert, R, Bessis, Y, Ville, M, Vekemans, M, Dommergues
المصدر: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 9(2)
مصطلحات موضوعية: Adult, Chromosome Aberrations, Fetoscopy, Gestational Age, Trisomy, Fetofetal Transfusion, Polymerase Chain Reaction, Ultrasonography, Prenatal, Congenital Abnormalities, Cytogenetics, Fetal Diseases, Fetus, Pregnancy, Risk Factors, Karyotyping, Prenatal Diagnosis, Amniocentesis, Drainage, Humans, Ethics, Medical, Female, In Situ Hybridization, Fluorescence, Maternal Age
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::e5475ba9fa6d10203930f07edfb5c168Test
https://pubmed.ncbi.nlm.nih.gov/11915501Test -
6
المؤلفون: A, Mégarbané, P, Gosset, N, Souraty, J M, Lapierre, R, Korban, L, Zahed, L, Samaras, M, Vekemans, M, Prieur
المصدر: American journal of medical genetics. 104(3)
مصطلحات موضوعية: Adult, Chromosome Aberrations, Male, Chromosomes, Human, Pair 10, Palate, Retrognathia, Flatfoot, Chromosome Banding, Gene Duplication, Intellectual Disability, Karyotyping, Humans, Abnormalities, Multiple, In Situ Hybridization, Fluorescence
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::0b97f4852858c1e91b8ab588766d9b08Test
https://pubmed.ncbi.nlm.nih.gov/11754045Test -
7
المؤلفون: K A, Rack, F, Salomon-Nguyen, I, Radford-Weiss, M O, Gil, C, Schmitt, C, Belanger, S, Nusbaum, M, Vekemans, F, Valensi, E A, Macintyre
المصدر: British journal of haematology. 103(2)
مصطلحات موضوعية: Chromosomes, Human, Pair 14, Karyotyping, Humans, Cell Separation, Chromosomes, Human, Pair 18, Flow Cytometry, Immunoglobulin Heavy Chains, Interphase, Lymphoma, Follicular, In Situ Hybridization, Fluorescence, Metaphase, Translocation, Genetic, Genes, bcl-2
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::c63ebae91a94eec15ddc477db8b432f3Test
https://pubmed.ncbi.nlm.nih.gov/9827925Test -
8
المؤلفون: K A, Rack, E, Delabesse, I, Radford-Weiss, P, Bourquelot, G, Le Guyader, M, Vekemans, E A, Macintyre
المصدر: Genes, chromosomescancer. 23(3)
مصطلحات موضوعية: Chromosomes, Human, Pair 14, Genes, Immunoglobulin, Lymphoma, Chromosomes, Human, Pair 22, Restriction Mapping, Genes, myc, Translocation, Genetic, Karyotyping, Proto-Oncogenes, Tumor Cells, Cultured, Humans, Immunoglobulin Constant Regions, Chromosomes, Artificial, Yeast, In Situ Hybridization, Fluorescence, Chromosomes, Human, Pair 8
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::8dd88246a5d452c957faba2f1f58e1d7Test
https://pubmed.ncbi.nlm.nih.gov/9790502Test -
9
المؤلفون: I. Radford-Weiss, Xavier Troussard, M Vekemans, Elisabeth Macintyre, Laurent Mauvieux, Richard Garand, Françoise Valensi, Rack K, G. Flandrin
المصدر: British journal of haematology. 101(4)
مصطلحات موضوعية: Male, medicine.medical_specialty, Pathology, Monosomy, Lymphoma, B-Cell, Lymphocytosis, Gene Rearrangement, B-Lymphocyte, Heavy Chain, Trisomy, Biology, Polymerase Chain Reaction, Translocation, Genetic, Immunophenotyping, hemic and lymphatic diseases, medicine, Humans, Cyclin D1, Aged, Chromosomes, Human, Pair 14, Chromosomes, Human, Pair 12, Chromosomes, Human, Pair 11, Splenic Neoplasms, Cytogenetics, Splenic lymphoma with villous lymphocytes, Hematology, Middle Aged, medicine.disease, Chromosome 3, Chromosomes, Human, Pair 2, Karyotyping, Mantle cell lymphoma, Female, Chromosomes, Human, Pair 3, CD5, medicine.symptom, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925f1f1350ee47bd4502eec9d4f272d9Test
https://pubmed.ncbi.nlm.nih.gov/9674745Test -
10
المؤلفون: A, Mégarbané, N, Souraty, D, Theophile, M, Vekemans, L, Samaras, Z, Ghorayeb
المصدر: Annales de genetique. 40(1)
مصطلحات موضوعية: Male, Chromosomes, Human, Pair 13, Child, Preschool, Face, Intellectual Disability, Karyotyping, Humans, Abnormalities, Multiple, Trisomy, Syndrome, Translocation, Genetic, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::d26bbbfffa4d7681df9fcfe6e2f49170Test
https://pubmed.ncbi.nlm.nih.gov/9150851Test