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Genetic Testing and Molecular Biomarkers|April 9, 2010
High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effectsMariem Ben Saïd, Mounira Hmani-Aifa, Imen Amar, et al.
Genetic Testing and Molecular Biomarkers|October 9, 2009
Significant genetic differentiation within the population of the Island of Corsica (France) revealed by y-chromosome analysisMaria Elena Ghiani, Laurent Varesi, Robert John Mitchell, et al.
Genetic Testing and Molecular Biomarkers|October 9, 2009
Single-nucleotide polymorphisms in genes encoding toll-like receptor -2, -3, -4, and -9 in case-control study with breast cancerGodfrey E Etokebe, Jelena Knezević, Branka Petricević, et al.
Genetic Testing and Molecular Biomarkers|October 9, 2009
Methylenetetrahydrofolate reductase and angiotensin-converting enzyme gene polymorphisms among Saudi population from Qassim regionAbdullah Algasham, Hisham Ismail, Moataz Dewaidar, et al.
Genetic Testing and Molecular Biomarkers|August 4, 2009
Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafnessShinji Kunishima, Tatsuo Matsunaga, Yoshimi Ito, et al.
Genetic Testing and Molecular Biomarkers|August 4, 2009
Low prevalence and variable clinical presentation of troponin I and troponin T gene mutations in hypertrophic cardiomyopathyKarol Curila, Lucie Benesova, Martin Penicka, et al.
Genetic Testing and Molecular Biomarkers|July 8, 2009
Genetic testing for inflammatory bowel disease: focus group analysis of patients and family membersJeffrey R Lewis, Vani Konda, David T Rubin
Genetic Testing and Molecular Biomarkers|August 12, 2009
Detection of non-DeltaGT NCF-1 mutations in chronic granulomatous diseaseMarianne Antonius Jakobsen, Svend Stenvang Pedersen, Torben Barington
Genetic Testing and Molecular Biomarkers|August 12, 2009
False homozygous deletions of SMN1 exon 7 using Dra I PCR-RFLP caused by a novel mutation in spinal muscular atrophySeong-Ho Kang, Sung Im Cho, Jong-Hee Chae, et al.
Genetic Testing and Molecular Biomarkers|March 8, 2011
Use of ethnicity-specific sequence tag site markers for Y chromosome microdeletion studiesKabir Sachdeva, Renu Saxena, Abha Majumdar, et al.
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