Showing results (1321-1330 of 3,522) with videos related to
Sort By:
Pageof 353
Journal of Human Genetics|February 21, 2007
Glucocorticoid-induced granzyme A expression can be used as a marker of glucocorticoid sensitivity for acute lymphoblastic leukemia therapyAkira Myoumoto, Kaoru Nakatani, Taka-Aki Koshimizu, et al.Journal of Human Genetics|March 28, 2007
Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphismsDaniela Zahorakova, Robert Rosipal, Jan Hadac, et al.Journal of Human Genetics|March 28, 2007
Association of a chromosome 1q21 locus in close proximity to a late cornified envelope-like proline-rich 1 (LELP1) gene with total serum IgE levelsMamta Sharma, Kamiya Mehla, Jyotsna Batra, et al.Journal of Human Genetics|February 8, 2007
Functional pathway characterized by gene expression analysis of supraclavicular lymph node metastasis-positive breast cancerYoko Oishi, Koichi Nagasaki, Satoshi Miyata, et al.Journal of Human Genetics|February 3, 2007
Systematic assessment of the tagging polymorphisms of the COL1A1 gene for high myopiaChung-Ling Liang, Kuo-Sheng Hung, Yueh-Ying Tsai, et al.Journal of Human Genetics|February 6, 2007
Expression and phylogenetic analyses of human endogenous retrovirus HC2 belonging to the HERV-T family in human tissues and cancer cellsJoo-Mi Yi, Heui-Soo KimJournal of Human Genetics|January 31, 2007
Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoterEsther N Maina, Tessa Webb, Sarita Soni, et al.Journal of Human Genetics|February 1, 2007
A Japanese case of oto-palato-digital syndrome type II: an apparent lack of phenotype-genotype correlationT Kondoh, N Okamoto, N Norimatsu, et al.Journal of Human Genetics|October 20, 2006
New splicing mutations in propionic acidemiaLourdes R Desviat, Sonia Clavero, Celia Perez-Cerdá, et al.Journal of Human Genetics|November 9, 2006
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assayValentina Gatta, Ivana Antonucci, Elisena Morizio, et al.Pageof 353