Articles
Volume 10 (2009) - October 2009
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Research article
Ceri E Stewart, Ian P Hall, Stuart G Parker, Miriam F Moffat, Andrew J Wardlaw, Martin J Connolly, Charlotte Ruse, Ian Sayers BMC Medical Genetics 2009, 10:112 (31 October 2009) |
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Research article
Suet Chen, Mehmet Cilingiroglu, Josh Todd, Raffaella Lombardi, James T Willerson, Antonio M Gotto, Christie M Ballantyne, AJ Marian BMC Medical Genetics 2009, 10:111 (30 October 2009) |
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Research article
Telomere shortening may be associated with human keloids Bruna De Felice, Robert R Wilson, Massimo Nacca BMC Medical Genetics 2009, 10:110 (28 October 2009) |
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Research article
Jiri Gallo, Frantisek Mrazek, Martin Petrek BMC Medical Genetics 2009, 10:109 (27 October 2009) |
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Research article
Audrey Y Chu, Rulan S Parekh, Brad C Astor, Josef Coresh, Yvette Berthier-Schaad, Michael W Smith, Alan R Shuldiner, Wen Kao BMC Medical Genetics 2009, 10:108 (23 October 2009) |
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Research article
Karolina Åberg, Feng Dai, Satupaitea Viali, John Tuitele, Guangyun Sun, Subba R Indugula, Ranjan Deka, Daniel E Weeks, Stephen T McGarvey BMC Medical Genetics 2009, 10:107 (23 October 2009) |
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Research article
Genetic effect of CysLTR2 polymorphisms on its mRNA synthesis and stabilization Jeong-Ah Shin, Hun Chang, Se-Min Park, An-Soo Jang, Sung Park, Jong Park, Soo-Taek Uh, Gune Il Lim, Taiyoun Rhim, Mi-Kyeong Kim, Inseon S Choi, Il Chung, Byung Park, Hyoung Shin, Choon-Sik Park BMC Medical Genetics 2009, 10:106 (20 October 2009) |
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Research article
Identification of a novel functional deletion variant in the 5'-UTR of the DJ-1 gene Rowena J Keyser, Lize van der Merwe, Mauritz Venter, Craig Kinnear, Louise Warnich, Jonathan Carr, Soraya Bardien BMC Medical Genetics 2009, 10:105 (13 October 2009) |
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Research article
The role of Danielle Carpenter, Christopher Ringrose, Vincenzo Leo, Andrew Morris, Rachel L Robinson, P Jane Halsall, Philip M Hopkins, Marie-Anne Shaw BMC Medical Genetics 2009, 10:104 (13 October 2009) Genotyping analysis of the largest cohort of patients with malignant hyperthermia to date identifies a potentially pathogenic change in the CACNA1S gene and highlights the variability of this gene among people with this skeletal muscle disorder.
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Research article
Lisa Gallicchio, Howard H Chang, Dana K Christo, Lucy Thuita, Han Huang, Paul Strickland, Ingo Ruczinski, Sandra Clipp, Kathy J Helzlsouer BMC Medical Genetics 2009, 10:103 (9 October 2009) |
