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Human Mutation|April 19, 2008
Sunlight ultraviolet irradiation and BRAF V600 mutagenesis in human melanomaAhmad Besaratinia, Gerd P PfeiferHuman Mutation|April 23, 2008
Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type IA Oshima, T Jaijo, E Aller, et al.Human Mutation|April 24, 2008
MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset casesStefanie Engert, Barbara Wappenschmidt, Beate Betz, et al.Human Mutation|March 12, 2008
Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH)Johan Staaf, Therese Törngren, Eva Rambech, et al.Human Mutation|March 12, 2008
Discovery of genetic profiles impacting response to chemotherapy: application to gemcitabineHamdi Jarjanazi, Jeffrey Kiefer, Sevtap Savas, et al.Human Mutation|May 7, 2008
Mutations and polymorphisms of the gene of the major human blood protein, serum albuminLorenzo Minchiotti, Monica Galliano, Ulrich Kragh-Hansen, et al.Human Mutation|May 13, 2008
The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disordersYoko Aoki, Tetsuya Niihori, Yoko Narumi, et al.Human Mutation|June 4, 2008
A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP geneDianalee A McKnight, P Suzanne Hart, Thomas C Hart, et al.Human Mutation|April 15, 2014
A dominant mutation in the stereocilia-expressing gene TBC1D24 is a probable cause for nonsyndromic hearing impairmentLuping Zhang, Lingxiang Hu, Yongchuan Chai, et al.Pageof 583