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| Kannan M, Ahmad F, Yadav BK, et al.
Carrier detection in glanzmann thrombasthenia: comparison of flow cytometry and Western blot with respect to DNA mutation. [Journal Article]
Am J Clin Pathol 2008 Jul; 130(1):93-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Losonczy G, Rosenberg N, Kiss C, et al.
A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIa. [Case Reports, Journal Article]
Thromb Haemost 2005 May; 93(5):904-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Jayo A, Pabón D, Lastres P, et al.
Type II Glanzmann thrombasthenia in a compound heterozygote for the alphaIIb gene. A novel missense mutation in exon 27. [Journal Article]
Haematologica 2006 Oct; 91(10):1352-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Hayashi T, Tanaka S, Hori Y, et al.
Insertion of a C in the exon 28 of integrin alphaIIb gene leading to a frameshift mutation is responsible for Glanzmann thrombasthenia in a Japanese case. [Case Reports, Journal Article]
J Thromb Haemost 2005 Mar; 3(3):489-96.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Gu J
[Carrier detection of Glanzmann's thrombasthenia by Taq I restriction fragment length polymorphism of GPIIIa gene] [Journal Article]
Zhonghua Yi Xue Za Zhi 1991 Dec; 71(12):680-2, 46.
Abstract | Full Citation | Find Related Articles | | Tanaka S, Hayashi T, Yoshimura K, et al.
Double heterozygosity for a novel missense mutation of Ile304 to Asn in addition to the missense mutation His280 to Pro in the integrin beta3 gene as a cause of the absence of platelet alphaIIbbeta3 in Glanzmann's thrombasthenia. [Case Reports, Journal Article]
J Thromb Haemost 2005 Jan; 3(1):68-73.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Xie J, Pabón D, Jayo A, et al.
Type I Glanzmann thrombasthenia caused by an apparently silent beta3 mutation that results in aberrant splicing and reduced beta3 mRNA. [Case Reports, Journal Article]
Thromb Haemost 2005 May; 93(5):897-903.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Nair S, Li J, Mitchell WB, et al.
Two new beta3 integrin mutations in Indian patients with Glanzmann thrombasthenia: localization of mutations affecting cysteine residues in integrin beta3. [Case Reports, Journal Article]
Thromb Haemost 2002 Sep; 88(3):503-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Jayandharan G, Nelson EJ, Baidya S, et al.
A new multiplex PCR and conformation sensitive gel electrophoresis strategy for mutation detection in the platelet glycoprotein alphabeta genes. [JOURNAL ARTICLE]
J Thromb Haemost 2006 Oct 31.
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