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Polymorphism, Single-Stranded Conformational journal articles from PubMed MEDLINE database

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Torkamanzehi A, Kuhnlein U 
Restriction fragment length and single strand conformational polymorphisms in chicken mitochondrial phosphoenol-pyruate carboxykinase gene and its association with egg production. [Journal Article, Research Support, Non-U.S. Gov't]
Pak J Biol Sci 2007 Nov 15; 10(22):4075-80.
Abstract | Full Citation
Onsori H, Hosseinpour MA, Montaser-Kouhsari S, et al. 
Identification of a novel missense mutation in exon 4 of the human factor VIII gene associated with sever hemophilia A patient. [Journal Article, Research Support, Non-U.S. Gov't]
Pak J Biol Sci 2007 Dec 1; 10(23):4299-302.
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Trojani A, Ripamonti CB, Penco S, et al. 
Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorphism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation. [Journal Article, Research Support, Non-U.S. Gov't]
Anticancer Res 2008 Sep-Oct; 28(5A):2745-51.
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Mölne J, Björquist P, Andersson K, et al. 
Blood group ABO antigen expression in human embryonic stem cells and in differentiated hepatocyte- and cardiomyocyte-like cells. [Journal Article, Research Support, Non-U.S. Gov't]
Transplantation 2008 Nov 27; 86(10):1407-13.
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Tanaka K, Kumaravel TS, Ihda S, et al. 
Characterization of late-arising chromosome aberrations in human B-cell lines established from alpha-ray- or gamma-ray-irradiated lymphocytes. [Journal Article]
Cancer Genet Cytogenet 2008 Dec; 187(2):112-24.
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Kim MS, Jeong EG, Chung YJ, et al. 
Absence of somatic mutation of a tumor suppressor gene eukaryotic translation elongation factor 1, epsilon-1 (EEF1E1), in common human cancers. [Letter, Research Support, Non-U.S. Gov't]
APMIS 2008 Sep; 116(9):832-3.
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Grabowski P, Schrader J, Wagner J, et al. 
Loss of Nuclear p27 Expression and Its Prognostic Role in Relation to Cyclin E and p53 Mutation in Gastroenteropancreatic Neuroendocrine Tumors. [Journal Article]
Clin Cancer Res 2008 Nov 15; 14(22):7378-84.
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Barashkov NA, Dzhemileva LU, Fedorova SA, et al. 
[Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia).] [JOURNAL ARTICLE]
Vestn Otorinolaringol 2008; (5):23-28.
Abstract | Full Citation
De Tommasi A, Luzzi S, D'Urso PI, et al. 
Molecular genetic analysis in a case of ganglioglioma: identification of a new mutation. [Journal Article]
Neurosurgery 2008 Nov; 63(5):976-80; discussion 980.
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Strnad M, Brajuskovic G, Strelic N, et al. 
Expression of programmed cell death proteins in patients with chronic myeloid leukemia. [Journal Article]
J BUON 2008 Jul-Sep; 13(3):403-8.
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