Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Amjad H, Hayat"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::858144689c8d6627a9f1cedc34e3bad7
https://pubmed.ncbi.nlm.nih.gov/28143941
https://pubmed.ncbi.nlm.nih.gov/28143941
Autor:
Keaney, Thomas, O'Connor, Louise, Krawczyk, Janusz, Abdelrahman, Moutaz A., Hayat, Amjad H., Murray, Margaret, O'Dwyer, Michael, Percy, Melanie, Langabeer, Stehpen, Haslam, Karl, Glynn, Barry, Mullen, Ciara, Keady, Evelyn, Lahiff, Sinéad, Smith, Terry J.
Publikováno v:
Journal of Clinical Pathology; Aug2017, Vol. 70 Issue 8, p662-668, 7p, 3 Charts, 3 Graphs