| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 18378852 [Unique ID], provided by the PubMed system | |
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| | 1 - 10 of 105 journal articles in the PubMed database | Email to a friend | | |
| Percy MJ, Beer PA, Campbell G, et al.
Novel Exon 12 mutations in the HIF2A gene associated with erythrocytosis. [JOURNAL ARTICLE]
Blood 2008 Mar 31.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Percy MJ
Familial erythrocytosis arising from a gain-of-function mutation in the HIF2A gene of the oxygen sensing pathway. [Journal Article]
Ulster Med J 2008 May; 77(2):86-8.
Abstract | Full Citation | Find Related Articles | | Percy MJ, Furlow PW, Lucas GS, et al.
A gain-of-function mutation in the HIF2A gene in familial erythrocytosis. [Case Reports, Journal Article, Research Support, N.I.H., Extramural]
N Engl J Med 2008 Jan 10; 358(2):162-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Pastore Y, Jedlickova K, Guan Y, et al.
Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia. [Case Reports, Journal Article]
Am J Hum Genet 2003 Aug; 73(2):412-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Perrotta S, Della Ragione F
The HIF2A gene in familial erythrocytosis. [Comment, Letter]
N Engl J Med 2008 May 1; 358(18):1966; author reply 1966-7.
Full Citation | Find Related Articles | | Eltzschig HK, El Kasmi KC, Eckle T
The HIF2A gene in familial erythrocytosis. [Comment, Letter]
N Engl J Med 2008 May 1; 358(18):1965-6; author reply 1966-7.
Full Citation | Find Related Articles | | Pastore YD, Jelinek J, Ang S, et al.
Mutations in the VHL gene in sporadic apparently congenital polycythemia. [Case Reports, Journal Article]
Blood 2003 Feb 15; 101(4):1591-5.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Al-Sheikh M, Moradkhani K, Lopez M, et al.
Disturbance in the HIF-1alpha pathway associated with erythrocytosis: Further evidences brought by frameshift and nonsense mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene. [JOURNAL ARTICLE]
Blood Cells Mol Dis 2007 Oct 12.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Percy MJ, Scott LM, Erber WN, et al.
The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels. [Journal Article]
Haematologica 2007 Dec; 92(12):1607-14.
Abstract | Full Citation | Find Related Articles |   |
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