Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sofia Sraidi"'
Congenital factor V deficiency (CFVD) is a rare coagulation disorder, also known as para hemophilia, that was first described by Owren in 1947. Until now, no specific protocols for the management of these patients have been established, owing to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f1800b541c5d0464b1261659833773b
Autor:
Sara Naim, Sofia Sraidi, Nisrine Khoubila, Mouna Lamchahab, Siham Charkaoui, Mohamed Rachid, Meryem Qachouh, Abdelah Madani
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 22:S346
Genetic defects play a major role in pathogenesis of the most of haematological malignancies, including cytogenetic abnormalities, gene mutations, and abnormal gene expression. Our knowledge about the genetics of haematological disorders has been dra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64068dfd8e36a9879d85c8b3d4a7212e
http://www.intechopen.com/articles/show/title/haematological-malignancies-overview-of-the-recent-progresses-in-genetics
http://www.intechopen.com/articles/show/title/haematological-malignancies-overview-of-the-recent-progresses-in-genetics
Publikováno v:
Cytogenetics-Classical and Molecular Strategies for Analysing Heredity Material ISBN: 9781839689413
Acute lymphoblastic leukemia (ALL), can be defined by a family of genetically heterogeneous lymphoid neoplasms derived from B- and T-lymphoid progenitors. ALL constitutes the most common childhood cancer, due to an overproduction of immature lymphoid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d54f06f3e28a9289eaee7081ddd3b28
http://www.intechopen.com/articles/show/title/genetic-abnormalities-in-all
http://www.intechopen.com/articles/show/title/genetic-abnormalities-in-all