المؤلفون: A.E. Dollin, P.A. Martin-DeLeon, G.R. Sutherland, K.K. Kidd, E. Calef, G. Utermann, S.J. O’Brien, J.R.K. Savage, G.A. Bonaminio, J. Egozcue, V. Greger, B. Porfirio, D. Caporossi, G. Kovacs, E. Baker, L. Wilkens, E. Gersdorf, J.D. Murray, R.K. Wayne, A.M. Estop, W.S. Modi, C. Frocrain-Herchkovitch, B. Horsthemke, B. Tedeschi, D.C. Morizot, V.J. Hyland, B. Nicoletti, F. Guilhot, R.I. Richards, B.A. Evans, J. Santalo, J.L. Huret, D.F. Callen, J. Wu, R.L. Close, J.A. Close, J.M. Lacson, T.G. Fanning, M.D.B. Eldridge, T. Miki, G.W. Tregear, V. Catala, N.S. Fechheimer, J.E. Womack, T. Papp, J. Gosálvez, P. Vernole, S.M. Zneimer, J. Tanzer, S.R. Picciano, W.K. Cavenee, V. Goyanes, D. Frezza, P.G. Johnston

المصدر: Cytogenetic and Genome Research. 48:I-IV

مصطلحات موضوعية: Botany, Genetics, Biology, Molecular Biology, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d5f4d5847674b1c9cb779272cdfba0e6
https://doi.org/10.1159/000132625

المؤلفون: J. Tanzer, J.R.K. Savage, F. Guilhot, Huret Jl, C. Frocrain-Herchkovitch

المصدر: Cytogenetic and Genome Research. 48:224-227

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Pathology, medicine.medical_specialty, X Chromosome, Aneuploidy, Chromosome Disorders, Chromosomal translocation, Biology, Bone Marrow, Fanconi anemia, Genetics, medicine, Humans, Lymphocytes, Molecular Biology, Sex Chromosome Aberrations, Genetics (clinical), X chromosome, Cell Nucleus, Chromosome Aberrations, Cytogenetics, Anemia, Aplastic, Karyotype, medicine.disease, Molecular biology, Fanconi Anemia, medicine.anatomical_structure, Chromosomes, Human, Pair 1, Karyotyping, Chromosomes, Human, Pair 5, Bone marrow, Trisomy

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d4b442cf18112479d94e0892616b609
https://doi.org/10.1159/000132633

المؤلفون: J, Fraisse, C, Frocrain-Herchkovitch, C, Turc-Carel

المصدر: La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris. 59(19)

مصطلحات موضوعية: Chromosome Aberrations, Leukemia, Myeloid, Acute, Leukemia, Karyotyping, Acute Disease, Humans, Chromosome Disorders, Prognosis, Chromosome Banding, Leukemia, Lymphoid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::0ef88637e4d60897a89edb03773965e6
https://pubmed.ncbi.nlm.nih.gov/6310764

المؤلفون: C, Frocrain-Herchkovitch

المصدر: La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris. 59(21)

مصطلحات موضوعية: Chromosome Aberrations, Chromosomes, Human, 6-12 and X, Male, Adolescent, Chromosome Disorders, Diploidy, Translocation, Genetic, Leukemia, Lymphoid, Child, Preschool, Karyotyping, Chromosomes, Human, 21-22 and Y, Humans, Female, Child, Chromosomes, Human, 13-15

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::8644372d1b119b7ebc0bc9f57ce69218
https://pubmed.ncbi.nlm.nih.gov/6310779

المؤلفون: J, Fraisse, C, Frocrain-Herchkovitch, C, Turc-Carel

المصدر: Pathologie-biologie. 30(9)

مصطلحات موضوعية: Chromosome Aberrations, Leukemia, Karyotyping, Acute Disease, Humans

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::4859247dd03973de7c0c225bf49f89b9
https://pubmed.ncbi.nlm.nih.gov/6760080

المؤلفون: C, Frocrain-Herchkovitch

المصدر: Pathologie-biologie. 30(9)

مصطلحات موضوعية: Chromosome Aberrations, Karyotyping, Humans, Translocation, Genetic, Leukemia, Lymphoid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::1f7ae527786e2eda2a24aad30afd64d1
https://pubmed.ncbi.nlm.nih.gov/6760083

المؤلفون: J. Dumont, C. Frocrain-Herchkovitch, Pierre Pouillart, A. Aurias, J.P. Thiery

المصدر: European Journal of Cancer and Clinical Oncology. 19:1270

مصطلحات موضوعية: Pathology, medicine.medical_specialty, Therapy related, Oncology, medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3552aeb27db1d4dfcb68d7e64dec2f1c
https://doi.org/10.1016/0277-5379(83)90213-4