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Genetic Testing and Molecular Biomarkers|April 14, 2010
Allele drop-out in the MECP2 gene due to G-quadruplex and i-motif sequences when using polymerase chain reaction-based diagnosis for Rett syndromeCarol J Saunders, Michael J Friez, Melanie Patterson, et al.
Genetic Testing and Molecular Biomarkers|June 29, 2010
The genetic background difference between diabetic patients with and without nephropathy in a Taiwanese population by linkage disequilibrium mapping using 382 autosomal STR markersDee Pei, Yi-Jen Huang, Chang-Hsun Hsieh, et al.
Genetic Testing and Molecular Biomarkers|July 21, 2010
Cytogenetic analysis of 1572 cases of Down syndrome: a report of double aneuploidy and novel findings 47,XY, t(14;21)(q13;q22.3)mat,+21 and 45,XX,t(14;21) in an Indian populationSwarna Mandava, Neeraja Koppaka, Vinay Bhatia, et al.
Genetic Testing and Molecular Biomarkers|August 21, 2010
Diagnosis of Down syndrome and detection of origin of nondisjunction by short tandem repeat analysisShalu Jain, Sarita Agarwal, Inusha Panigrahi, et al.
Genetic Testing and Molecular Biomarkers|August 21, 2010
Absence of commonly reported leucine-rich repeat kinase 2 mutations in Eastern Indian Parkinson's disease patientsJaya Sanyal, Biswanath Sarkar, Sabyasachi Ojha, et al.
Genetic Testing and Molecular Biomarkers|August 21, 2010
Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing lossDaniela Tiaki Uehara, Daniel Rincon, Ronaldo Serafim Abreu-Silva, et al.
Genetic Testing and Molecular Biomarkers|July 24, 2010
Oxidative stress, Helicobacter pylori, and OGG1 Ser326Cys, XPC Lys939Gln, and XPD Lys751Gln polymorphisms in a Turkish population with colorectal carcinomaAyse Basak Engin, Bensu Karahalil, Atilla Engin, et al.
Genetic Testing and Molecular Biomarkers|December 15, 2010
Proposed algorithm for the best detection of different bcr-abl gene fusion transcripts in molecular diagnostics laboratories: experience of a major referral centerRouba Hoteit, Rami Mahfouz
Genetic Testing and Molecular Biomarkers|November 25, 2010
Single-nucleotide polymorphisms of NKX2.5 found in congenital heart disease patients of Mysore, South IndiaS M Dinesh, L Kusuma, R Smitha, et al.
Genetic Testing and Molecular Biomarkers|October 14, 2010
Association of methylenetetrahydrofolate reductase C677T and cystathionine β-synthase polymorphisms in cardiovascular disease in the algerian populationBakhouche Houcher, Zahira Houcher, Abderrezak Touabti, et al.
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