المؤلفون: R. Valli, L. Vinti, A. Frattini, M. Fabbri, G. Montalbano, C. Olivieri, A. Minelli, F. Locatelli, F. Pasquali, E. Maserati

المصدر: Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)

مصطلحات موضوعية: Severe aplastic anaemia, Pancytopenia, Chromosome structural anomalies, Chromosome 8, Chromosome 2, RUNX1T1 gene, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s13039-017-0352-2Test; https://doaj.org/toc/1755-8166Test

الوصول الحر: https://doaj.org/article/2f5a69225cd044c6b91e874bb142ae0bTest

المؤلفون: Locatelli, Franco

المساهمون: Marletta, Cristina, Valli, Roberto, Pressato, Barbara, Mare, Lydia, Montalbano, Giuseppe, Menna, Giuseppe, Loffredo, Giuseppe, Bernardo, Maria Ester, Vinti, Luciana, Ferrari, Simona, Di Cesare-Merlone, Alessandra, Zecca, Marco, Lo Curto, Francesco, Locatelli, Franco, Pasquali, Francesco, Maserati, Emanuela

مصطلحات موضوعية: SAA, Thrombocytopenia, CAMT, RUNX1, MPL, Chromosome structural anomalies, Chromosome 1, Chromosome 21, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23025896; info:eu-repo/semantics/altIdentifier/wos/WOS:000314608400001; volume:5; issue:1; firstpage:N/A; lastpage:N/A; issueyear:2012; journal:MOLECULAR CYTOGENETICS; https://hdl.handle.net/10807/244815Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84866779821

الإتاحة: https://doi.org/10.1186/1755-8166-5-39Test
https://hdl.handle.net/10807/244815Test

المؤلفون: Marletta Cristina, Valli Roberto, Pressato Barbara, Mare Lydia, Montalbano Giuseppe, Menna Giuseppe, Loffredo Giuseppe, Bernardo Maria, Vinti Luciana, Ferrari Simona, Di Cesare-Merlone Alessandra, Zecca Marco, Lo Curto Francesco, Locatelli Franco, Pasquali Francesco, Maserati Emanuela

المصدر: Molecular Cytogenetics, Vol 5, Iss 1, p 39 (2012)

مصطلحات موضوعية: SAA, Thrombocytopenia, CAMT, RUNX1, MPL, Chromosome structural anomalies, Chromosome 1, Chromosome 21, Genetics, QH426-470

العلاقة: http://www.molecularcytogenetics.org/content/5/1/39Test; https://doaj.org/toc/1755-8166Test; https://doaj.org/article/dbabfb74951d42279dd698f7cee5425eTest

الإتاحة: https://doi.org/10.1186/1755-8166-5-39Test
https://doaj.org/article/dbabfb74951d42279dd698f7cee5425eTest

المؤلفون: Luciana Vinti, Francesco Pasquali, Antonella Minelli, Emanuela Maserati, Francesco Locatelli, Marco Fabbri, Giuseppe Montalbano, Annalisa Frattini, Roberto Valli, Carla Olivieri

المصدر: Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Chromosome 2, Chromosome 8, Chromosome structural anomalies, Pancytopenia, RUNX1T1 gene, Severe aplastic anaemia, Biochemistry, Molecular Medicine, Molecular Biology, Genetics, Genetics (clinical), Biochemistry (medical), lcsh:QH426-470, chromosome 2, chromosome 8, chromosome structural anomalies, pancytopenia, severe aplastic anaemia, Neutropenia, Gastroenterology, Chromosome aberration, 03 medical and health sciences, Internal medicine, hemic and lymphatic diseases, medicine, Aplastic anemia, medicine.diagnostic_test, Psychomotor retardation, business.industry, Bone marrow failure, Cytogenetics, medicine.disease, lcsh:Genetics, 030104 developmental biology, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, medicine.symptom, business, Fluorescence in situ hybridization

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::646ee570962adaf6b7863688d2eff6eeTest
https://hdl.handle.net/10807/229970Test

المؤلفون: Marletta, Cristina, Valli, Roberto, Pressato, Barbara, Mare, Lydia, Montalbano, Giuseppe, Menna, Giuseppe, Loffredo, Giuseppe, Bernardo, Maria, Vinti, Luciana, Ferrari, Simona, Di Cesare-Merlone, Alessandra, Zecca, Marco, Lo Curto, Francesco, Locatelli, Franco, Pasquali, Francesco, Maserati, Emanuela

مصطلحات موضوعية: SAA, Thrombocytopenia, CAMT, RUNX1, MPL, Chromosome structural anomalies, Chromosome 1, Chromosome 21

العلاقة: http://www.molecularcytogenetics.org/content/5/1/39Test

الإتاحة: http://www.molecularcytogenetics.org/content/5/1/39Test

المؤلفون: Locatelli F.

المساهمون: Valli, R., Vinti, L., Frattini, A., Fabbri, M., Montalbano, G., Olivieri, C., Minelli, A., Locatelli, Franco, Pasquali, F., Maserati, E.

مصطلحات موضوعية: Chromosome 2, Chromosome 8, Chromosome structural anomalies, Pancytopenia, RUNX1T1 gene, Severe aplastic anaemia, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000422750900001; volume:11; issue:1; firstpage:1; lastpage:9; numberofpages:9; issueyear:2018; journal:MOLECULAR CYTOGENETICS; https://hdl.handle.net/10807/229970Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85040461900

الإتاحة: https://doi.org/10.1186/s13039-017-0352-2Test
https://hdl.handle.net/10807/229970Test

المؤلفون: R, Valli, L, Vinti, A, Frattini, M, Fabbri, G, Montalbano, C, Olivieri, A, Minelli, F, Locatelli, F, Pasquali, E, Maserati

المصدر: Molecular Cytogenetics

مصطلحات موضوعية: Chromosome 8, Pancytopenia, Chromosome structural anomalies, hemic and lymphatic diseases, Research, RUNX1T1 gene, Chromosome 2, Severe aplastic anaemia

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::f982022220ba282640c10560de0611f2Test
https://pubmed.ncbi.nlm.nih.gov/29344089Test

المؤلفون: Lydia Mare, Giuseppe Loffredo, Maria Ester Bernardo, Marco Zecca, Roberto Valli, Alessandra Di Cesare-Merlone, Barbara Pressato, Luciana Vinti, Emanuela Maserati, Giuseppe Montalbano, Cristina Marletta, Franco Locatelli, Giuseppe Menna, Francesco Pasquali, Simona Ferrari, Francesco Lo Curto

المساهمون: Marletta, C., Valli, R., Pressato, B., Mare, L., Montalbano, G., Menna, G., Loffredo, G., Bernardo, M. E., Vinti, L., Ferrari, S., Di Cesare-Merlone, A., Zecca, M., Lo Curto, F., Locatelli, F., Pasquali, F., Maserati, E.

المصدر: Molecular Cytogenetics, Vol 5, Iss 1, p 39 (2012)
Molecular Cytogenetics

مصطلحات موضوعية: medicine.medical_specialty, RUNX1, lcsh:QH426-470, MPL, Biochemistry, chemistry.chemical_compound, Chromosome structural anomalies, hemic and lymphatic diseases, Genetics, medicine, Genetics(clinical), Molecular Biology, Genetics (clinical), Biochemistry, medical, Cytopenia, business.industry, Research, Biochemistry (medical), Cytogenetics, Chromosome 1, Chromosome, medicine.disease, Thrombocytopenia, SAA, Human genetics, Peripheral, Chromosome 21, lcsh:Genetics, medicine.anatomical_structure, chemistry, Immunology, CAMT, Molecular Medicine, Bone marrow, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de660cac88b5a8840648876e2ccf1e44Test
https://doi.org/10.1186/1755-8166-5-39Test

مصطلحات الفهرس: Chromosome 2, Chromosome 8, Chromosome structural anomalies, Pancytopenia, RUNX1T1 gene, Severe aplastic anaemia, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, info:eu-repo/semantics/article

URL: https://hdl.handle.net/10807/229970Test
info:eu-repo/semantics/altIdentifier/wos/WOS:000422750900001
volume:11
issue:1
firstpage:1
lastpage:9
numberofpages:9
issueyear:2018
journal:MOLECULAR CYTOGENETICS

مصطلحات الفهرس: SAA, Thrombocytopenia, CAMT, RUNX1, MPL, Chromosome structural anomalies, Chromosome 1, Chromosome 21, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, info:eu-repo/semantics/article

URL: https://hdl.handle.net/10807/244815Test
info:eu-repo/semantics/altIdentifier/pmid/23025896
info:eu-repo/semantics/altIdentifier/wos/WOS:000314608400001
volume:5
issue:1
firstpage:N/A
lastpage:N/A
issueyear:2012
journal:MOLECULAR CYTOGENETICS