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Genetic Testing and Molecular Biomarkers|June 27, 2017
The SDF1 A/G Gene Variant: A Susceptibility Variant for Myocardial InfarctionYaser Mansoori, Abdolreza Daraei, Zahra Zendebad, et al.
Genetic Testing and Molecular Biomarkers|June 27, 2017
Association of CCR2 (+190 G/A) Gene Variants and Ovarian Cancer SeverityGazi Yildirim, Rukset Attar, Seda Gulec-Yilmaz, et al.
Genetic Testing and Molecular Biomarkers|March 2, 2010
Analysis of CLCN2 as candidate gene for megalencephalic leukoencephalopathy with subcortical cystsGert C Scheper, Carola G M van Berkel, Lilia Leisle, et al.
Genetic Testing and Molecular Biomarkers|March 2, 2010
Mutations of the phenylalanine hydroxylase gene in Iranian Azeri Turkish patients with phenylketonuriaMortaza Bonyadi, Omid Omrani, Shiva Mohamadi Moghanjoghi, et al.
Genetic Testing and Molecular Biomarkers|February 9, 2010
The Italian external quality control program for familial adenomatous polyposis of the colon: five years of experienceFederica Censi, Vincenzo Falbo, Giovanna Floridia, et al.
Genetic Testing and Molecular Biomarkers|February 9, 2010
Williams-Beuren syndrome: diagnosis by polymorphic markersIvanete C Sbruzzi, Alexandre C Pereira, Beatriz Vasconcelos, et al.
Genetic Testing and Molecular Biomarkers|December 23, 2009
Cytogenetic and antineoplastic effects of modified steroidal alkylatorsIrini Karapidaki, Athanasios Papageorgiou, George Geromichalos, et al.
Genetic Testing and Molecular Biomarkers|April 10, 2018
PROGINS Polymorphism of the Progesterone Receptor Gene and the Susceptibility to Uterine Leiomyomas: A Systematic Review and Meta-AnalysisFlorinda da Silva, Noel Pabalan, Niramai Ekaratcharoenchai, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descentChai Saechao, Yadira Valles-Ayoub, Saghi Esfandiarifard, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
Detection of large rearrangements in the cystic fibrosis transmembrane conductance regulator gene by multiplex ligation-dependent probe amplification assay when sequencing fails to detect two disease-causing mutationsAnnika M Svensson, Lan-Szu Chou, Christine E Miller, et al.
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