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Journal of the American College of Cardiology|October 2, 2002
Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathyJinong Feng, Jin Yan Yan, Carolyn H Buzin, et al.
Mutation Research|September 29, 2004
Spontaneous multiple mutations show both proximal spacing consistent with chronocoordinate events and alterations with p53-deficiencyKathleen A Hill, Jicheng Wang, Kelly D Farwell, et al.
Environmental and Molecular Mutagenesis|October 14, 2003
Single-cell immunohistochemical mutation load assay (SCIMLA) using human paraffin-embedded tissuesGudrun Schlake, Qiang Liu, Ernst Heinmöller, et al.
Clinical and Experimental Dermatology|April 16, 1998
Investigation of the mechanism of action of 2% fusidic acid lotion in the treatment of acne vulgarisS Sommer, R Bojar, W J Cunliffe, et al.
Mitochondrion|December 29, 2010
Fibroblast immuno-diagnosis of cytochrome oxidase (COX) deficiency in mitochondrial diseaseAilian Du, Robert K Naviaux, Thuy Le, et al.
American Journal of Medical Genetics|March 15, 1994
Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenicsN M Lindor, J L Sobell, L L Heston, et al.
American Journal of Medical Genetics|February 16, 1996
Genotype-to-phenotype analysis: search for clinical characteristics of a missense change in the GABAA-beta 1 receptor geneJ L Sobell, D C Sigurdson, L L Heston, et al.
Molecular & General Genetics : MGG|November 1, 1988
PsiB polypeptide prevents activation of RecA protein in Escherichia coliA Bailone, A Bäckman, S Sommer, et al.
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