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1دورية أكاديمية
المؤلفون: Pellegrino B., Cavanna L., Boggiani D., Zamagni C., Frassoldati A., Schirone A., Caldara A., Rocca A., Gori S., Piacentini F., Berardi R., Brandes A. A., Foglietta J., Villa F., Todeschini R., Tognetto M., Naldi N., Bortesi B., Montemurro F., Ardizzoni A., Boni L., Musolino A.
المساهمون: Pellegrino B., Cavanna L., Boggiani D., Zamagni C., Frassoldati A., Schirone A., Caldara A., Rocca A., Gori S., Piacentini F., Berardi R., Brandes A.A., Foglietta J., Villa F., Todeschini R., Tognetto M., Naldi N., Bortesi B., Montemurro F., Ardizzoni A., Boni L., Musolino A.
مصطلحات موضوعية: breast cancer, eribulin, gemcitabine, metastatic, pharmacogenetic, TNBC, Antineoplastic Combined Chemotherapy Protocol, Deoxycytidine, Female, Furan, Human, Ketone, Microfilament Protein, Prospective Studie, Triple Negative Breast Neoplasms
وصف الملف: ELETTRONICO
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33399082; info:eu-repo/semantics/altIdentifier/wos/WOS:000631402900017; volume:6; issue:1; firstpage:1; lastpage:8; numberofpages:8; journal:ESMO OPEN; http://hdl.handle.net/11585/851662Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85100641127; https://doi.org/10.1016/j.esmoop.2020.100019Test
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2دورية أكاديمية
المؤلفون: Ansari, Morad, Rainger, Jacqueline K., Murray, Jennie E., Hanson, Isabel, Firth, Helen V., Mehendale, Felicity, Amiel, Jeanne, Gordon, Christopher T., Percesepe, Antonio, Fryer, Alan, Ferrari, Paola, Devriendt, Koenraad, Temple, I. Karen, Fitzpatrick, David R., MAZZANTI, LAURA
المساهمون: Ansari, Morad, Rainger, Jacqueline K., Murray, Jennie E., Hanson, Isabel, Firth, Helen V., Mehendale, Felicity, Amiel, Jeanne, Gordon, Christopher T., Percesepe, Antonio, Mazzanti, Laura, Fryer, Alan, Ferrari, Paola, Devriendt, Koenraad, Temple, I. Karen, Fitzpatrick, David R.
مصطلحات موضوعية: 5q deletion, Congenital contractural arachnodactyly, Fibrillin 2 (FBN2), Phosphorylated adaptor for RNA export (PHAX), Pierre Robin sequence, Talipes equinovaru, Adolescent, Child, Cleft Palate, Clubfoot, Contracture, Ear, External, Female, Finger, Haploinsufficiency, Human, Male, Microfilament Protein, Mutation, Missense, Nucleocytoplasmic Transport Protein, Phenotype, Phosphoprotein, Pierre Robin Syndrome, Sequence Deletion, Syndrome, Young Adult, Chromosomes, Pair 5
وصف الملف: ELETTRONICO
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25195018; info:eu-repo/semantics/altIdentifier/wos/WOS:000343331200009; volume:57; issue:10; firstpage:587; lastpage:595; numberofpages:9; journal:EUROPEAN JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11585/528167Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84908210018; http://www.elsevier.com/wps/find/journaldescription.cws_home/705239/description#descriptionTest
الإتاحة: https://doi.org/10.1016/j.ejmg.2014.08.007Test
http://hdl.handle.net/11585/528167Test
http://www.elsevier.com/wps/find/journaldescription.cws_home/705239/description#descriptionTest
