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Items: 2

1.
MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations
Daniela De Rocco, Barbara Zieger, Helen Platokouki, Paula G. Heller, Annalisa Pastore, Roberta Bottega, Patrizia Noris, Serena Barozzi, Ana C. Glembotsky, Helen Pergantou, Carlo L. Balduini, Anna Savoia, Alessandro Pecci
Eur J Med Genet. 2013 Jan; 56(1): 7–12. doi: 10.1016/j.ejmg.2012.10.009
PMCID:
PMC3546164
AbstractArticle
2.
Fine Expression Profiling of Full-length Transcripts using a Size-unbiased cDNA Library Prepared with the Vector-capping Method
Mio Oshikawa, Yoshiko Sugai, Ron Usami, Kuniyo Ohtoko, Shigeru Toyama, Seishi Kato
DNA Res. 2008 Jun; 15(3): 123–136. Published online 2008 May 16. doi: 10.1093/dnares/dsn010
PMCID:
PMC2650634
AbstractArticlePDF–265K

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