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Human Mutation|April 27, 2004
Proofreading genotyping assays and electrochemical detection of SNPsGarry C King, Daniel A Di Giusto, Wjatschesslaw A Wlassoff, et al.Human Mutation|April 27, 2004
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)Carsten Bergmann, Jan Senderek, Fabian Küpper, et al.Human Mutation|April 27, 2004
Novel mutations in the TRIM37 gene in Mulibrey NanismRiikka H Hämäläinen, Kristiina Avela, Julie A Lambert, et al.Human Mutation|June 29, 2004
DFold: PCR design that minimizes secondary structure and optimizes downstream genotyping applicationsDavid Fredman, M Jobs, L Strömqvist, et al.Human Mutation|June 29, 2004
Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouseNicolas Gilbert, Jamee M Bomar, Margit Burmeister, et al.Human Mutation|June 29, 2004
Haplotypes of the angiotensin II receptor genes AGTR1 and AGTR2 in women with normotensive pregnancy and women with preeclampsiaSally Plummer, Clare Tower, Pedro Alonso, et al.Human Mutation|June 29, 2004
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?M Fanin, L Fulizio, A C Nascimbeni, et al.Human Mutation|June 29, 2004
Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostosesStefan J White, Geraldine R Vink, Marjolein Kriek, et al.Human Mutation|June 29, 2004
TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed heartsStella Marie Reamon-Buettner, Juergen BorlakHuman Mutation|June 29, 2004
Screening of 25 Italian patients with Niemann-Pick A reveals fourteen new mutations, one common and thirteen private, in SMPD1V Ricci, M Stroppiano, F Corsolini, et al.Pageof 583