المؤلفون: Gianfranco Croci, Stefania Cesari, Michael B. Petersen, Emmanouil Manolakos, Angela Iasci, Loretta Thomaidis, Annalisa Vetro, Fabrizia Franchi, Orsetta Zuffardi, Maria Marinelli, Giulia Arrigo, Babara Dal Bello, Thomas Liehr, Emanuela Meneghelli

المصدر: European Journal of Medical Genetics. 55:185-190

مصطلحات موضوعية: Adult, Male, Telomere capture, Conventional cytogenetics, Array-CGH, Marker chromosome, Prenatal diagnosis, Trisomy, Biology, Germline, Fetus, FISH, Intellectual Disability, Genetics, Chromosomes, Human, Humans, Genetics(clinical), Supernumerary, Child, Small supernumerary marker chromosome, In Situ Hybridization, Fluorescence, Genetics (clinical), Comparative Genomic Hybridization, Partial Trisomy, Supernumerary marker chromosome, Infant, Newborn, Chromosome, General Medicine, Fish , Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f4f7c2141f230c8c691157258b5fcf6
https://doi.org/10.1016/j.ejmg.2012.01.010

المؤلفون: Daniela Giardino, Cecilia Corti, Lucia Ballarati, Daniela Colombo, Elena Sala, Nicoletta Villa, Giuseppe Piombo, Mauro Pierluigi, Francesca Faravelli, Silvana Guerneri, Domenico Coviello, Faustina Lalatta, Ugo Cavallari, Daniela Bellotti, Sergio Barlati, Gianfranco Croci, Fabrizia Franchi, Elisa Savin, Gianfranco Nocera, Francesco Paolo Amico, Paola Granata, Rosario Casalone, Lucia Nutini, Ermanna Lisi, Francesca Torricelli, Ursula Giussani, Barbara Facchinetti, Ginevra Guanti, Marilena Di Giacomo, Francesco Paolo Susca, Vanna Pecile, Lorenza Romitti, Laura Cardarelli, Erika Racalbuto, Maria Adalgisa Police, Francamaria Chiodo, Ornella Rodeschini, Patrizia Falcone, Emilio Donti, Maria Grazia Grimoldi, Emanuela Martinoli, Sabine Stioui, Daniele Caufin, Salvatrice Antonia Lauricella, Salvatrice Antonella Tanzariello, Gianfranco Voglino, Elisabetta Lenzini, Marco Besozzi, Lidia Larizza, Leda Dalprà

المصدر: Prenatal Diagnosis. 29:257-265

مصطلحات موضوعية: Genetics, Amniotic fluid, Chromosomal fragile site, Obstetrics and Gynecology, Chromosome, Prenatal diagnosis, Chromosomal translocation, Chromosome Fragility, Biology, medicine.anatomical_structure, Chromosome 3, medicine, Chorionic villi, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3f75a55a51e0e34f9641ea2b38e94f06
https://doi.org/10.1002/pd.2215

المؤلفون: Anna Baroncini, Francesca Rivieri, Antonella Capucci, Gianfranco Croci, Fabrizia Franchi, Paola Battaglia, SENSI, Alberto, AIELLO, Vincenzo, CALZOLARI, Elisa

المساهمون: Anna, Baroncini, Francesca, Rivieri, Antonella, Capucci, Gianfranco, Croci, Fabrizia, Franchi, Sensi, Alberto, Paola, Battaglia, Aiello, Vincenzo, Calzolari, Elisa

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/16378923; info:eu-repo/semantics/altIdentifier/wos/WOS:000234661800003; volume:48; firstpage:388; lastpage:396; numberofpages:8; journal:EUROPEAN JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11392/522660; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-29544447524

الاتاحة: http://hdl.handle.net/11392/522660

المؤلفون: Fabrizia Franchi, Anna Butturini, Enrichetta Bonilauri, Gianfranco Croci, M.Teresa Tondelli, Giancarlo Izzi, M. Alessandra Santucci, Alessandro Castriota Scanderbeg

المصدر: Leukemia Research. 15:759-763

مصطلحات موضوعية: Male, Interleukin 2, Cancer Research, Acute myeloblastic leukemia, Neutrophils, medicine.medical_treatment, Interferon-gamma, Myelogenous, Bone Marrow, Antineoplastic Combined Chemotherapy Protocols, Humans, Medicine, Interferon gamma, Bone Marrow Transplantation, Chemotherapy, business.industry, Cytarabine, Hematology, Immunotherapy, medicine.disease, Combined Modality Therapy, Leukemia, Myeloid, Acute, Leukemia, Oncology, Child, Preschool, Immunology, Cancer research, Interleukin-2, Female, business, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fda36160bde6aadcb9feed1f4c481d8
https://doi.org/10.1016/0145-2126(91)90080-d

المؤلفون: Gianfranco Croci, A. Sensi, V. Aiello, Paola Battaglia, Anna Baroncini, Francesca Rivieri, Fabrizia Franchi, Antonella Capucci, Elisa Calzolari

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Chromosomal translocation, Biology, Gastroenterology, Intellectual Disability, Internal medicine, Genetics, medicine, Chromosomes, Human, Humans, Family history, Child, In Situ Hybridization, Fluorescence, Genetics (clinical), Chromosome Aberrations, Gene Rearrangement, medicine.diagnostic_test, Infant, Newborn, Cytogenetics, Infant, Karyotype, General Medicine, Gene rearrangement, Middle Aged, Telomere, Subtelomere, Human genetics, Child, Preschool, Karyotyping, Female, Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c112ee681e0b02659cfb0cc0cf5c0a5
http://hdl.handle.net/11392/522660

المؤلفون: Leda Dalprà, Daniela Giardino, Palma Finelli, Cecilia Corti, Chiara Valtorta, Silvana Guerneri, Patrizia Ilardi, Renato Fortuna, Domenico Coviello, Gianfranco Nocera, Francesco Paolo Amico, Emanuela Martinoli, Elena Sala, Nicoletta Villa, Francesca Crosti, Francamaria Chiodo, Ludovica Verdun di Cantogno, Elisa Savin, Gianfranco Croci, Fabrizia Franchi, Giovanna Venti, Emilio Donti, Valeria Migliori, Antonella Pettinari, Stefania Bonifacio, Claudia Centrone, Francesca Torricelli, Simona Rossi, Paolo Simi, Paola Granata, Rosario Casalone, Elisabetta Lenzini, Lina Artifoni, Vanna Pecile, Sergio Barlati, Daniela Bellotti, Daniele Caufin, Adalgisa Police, Simona Cavani, Giuseppe Piombo, Mauro Pierluigi, Lidia Larizza

المساهمون: Dalpra', L, Giardino, D, Finelli, P, Corti, C, Valtorta, C, Guerneri, S, Ilardi, P, Fortuna, R, Coviello, D, Nocera, G, Amico, F, Martinoli, E, Sala, E, Villa, N, Crosti, F, Chiodo, F, di Cantogno, L, Savin, E, Croci, G, Franchi, F, Venti, G, Donti, E, Migliori, V, Pettinari, A, Bonifacio, S, Centrone, C, Torricelli, F, Rossi, S, Simi, P, Granata, P, Casalone, R, Lenzini, E, Artifoni, L, Pecile, V, Barlati, S, Bellotti, D, Caufin, D, Police, A, Cavani, S, Piombo, G, Pierluigi, M, Larizza, L

مصطلحات موضوعية: Genetics, Chromosome Aberrations, medicine.diagnostic_test, Neocentromere, supernumerary marker chromosomes, cooperative study, genotype–phenotype correlations, prenatal diagnosis, genetic counseling, Genetic counseling, Isochromosome, Inheritance Patterns, Chromosome, Prenatal diagnosis, Biology, Dicentric chromosome, Phenotype, Italy, medicine, Humans, Supernumerary, Genetic Testing, Genetics (clinical), In Situ Hybridization, Fluorescence, Genetic testing

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::624fc5449efab3a5dfa3ee4dbddb64a2
http://hdl.handle.net/11379/26069

المؤلفون: Elisabetta Manenti, Paola Rossi, Giuseppe Gobbi, Rodolfo Grazia, Andrea Tullini, Iria Neri, Annalisa Patrizi, Gianfranco Croci

المصدر: American Journal of Medical Genetics. 45:120-121

مصطلحات موضوعية: Pathology, medicine.medical_specialty, business.industry, medicine, Trisomy, medicine.disease, business, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7007f28ae1ed60d1fa126aea4ff81ebd
https://doi.org/10.1002/ajmg.1320450134

المؤلفون: Marco Buia, Sergio Maccari, Angelo Cesare Plancher, Laura Scarduelli, Casimiro Tramaloni, Gianfranco Croci, Carlo Di Donato, Stefano Lazzari, Roberto Vignoli

المصدر: American Journal of Clinical Pathology. 85:369-371

مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, Neutrophils, Chromosomes, Human, 19-20, Chronic neutrophilic leukemia, Trisomy, Chromosome 9, Disease, Biology, Bone marrow aspirate, Bone Marrow, medicine, Humans, Aged, Chromosome Aberrations, Chromosomes, Human, 6-12 and X, Karyotype, General Medicine, medicine.disease, Leukemia, Leukemia, Myeloid, Karyotyping, Immunology, Chromosome Deletion, Chromosome 20

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb77070c3b0aaa2f890885cf3648273
https://doi.org/10.1093/ajcp/85.3.369

المؤلفون: Fabrizia Franchi, C. Tarocco, Gianfranco Croci

المساهمون: Revues Inra, Import

المصدر: Génétique, Sélection, Évolution
Genetics Selection Evolution, Vol 19, Iss 3, Pp 381-386 (1987)

مصطلحات موضوعية: Genetics, lcsh:QH426-470, BOAR, Research, Chromosomal translocation, General Medicine, [SDV.GEN.GA] Life Sciences [q-bio]/Genetics/Animal genetics, Biology, lcsh:Genetics, Genetics(clinical), Animal Science and Zoology, lcsh:Animal culture, Ecology, Evolution, Behavior and Systematics, ComputingMilieux_MISCELLANEOUS, lcsh:SF1-1100

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e15f0d24e8b74e17689519c84feaedc
https://hal.archives-ouvertes.fr/hal-00893731