Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Stehpen, Langabeer"'
Autor:
Ciara Mullen, Janusz Krawczyk, Sinead Lahiff, Michael O'Dwyer, Evelyn Keady, Moutaz A Abdelrahman, Thomas Keaney, Stehpen Langabeer, Amjad Hayat, Karl Haslam, Terry J. Smith, Louise O'Connor, Barry Glynn, Margaret Murray, Melanie J. Percy
Publikováno v:
Journal of Clinical Pathology. 70:662-668
Aims Somatic insertions/deletions in exon 9 of the calreticulin gene have been identified in patients with essential thrombocythemia and primary myelofibrosis. Over 55 mutations have been discovered, 80% of which consist of either type 1 52-bp deleti
Autor:
Thomas, Keaney, Louise, O'Connor, Janusz, Krawczyk, Moutaz A, Abdelrahman, Amjad H, Hayat, Margaret, Murray, Michael, O'Dwyer, Melanie, Percy, Stehpen, Langabeer, Karl, Haslam, Barry, Glynn, Ciara, Mullen, Evelyn, Keady, Sinéad, Lahiff, Terry J, Smith
Publikováno v:
Journal of clinical pathology. 70(8)
Somatic insertions/deletions in exon 9 of the calreticulin gene have been identified in patients with essential thrombocythemia and primary myelofibrosis. Over 55 mutations have been discovered, 80% of which consist of either type 1 52-bp deletion or