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Journal of Human Genetics|April 27, 2001
Evaluation of RP2 and RP3 genes in an X-linked RP family manifesting loss of central vision and preserved peripheral functionM Hiraoka, M T Trese, B S ShastryJournal of Human Genetics|May 13, 1999
Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiencyY Suzuki, Z Zhang, N Shimozawa, et al.Journal of Human Genetics|May 13, 1999
Position-independent human beta-globin gene expression mediated by a recombinant adeno-associated virus vector carrying the chicken beta-globin insulatorT Inoue, H Yamaza, Y Sakai, et al.Journal of Human Genetics|May 13, 1999
Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) geneM Emi, N Keicho, K Tokunaga, et al.Journal of Human Genetics|May 13, 1999
Significantly elevated expression of PF4 (platelet factor 4) and eotaxin in the NOA mouse, a model for atopic dermatitisO Watanabe, K Natori, M Tamari, et al.Journal of Human Genetics|May 13, 1999
Cloning, tissue expression, and chromosomal assignment of human MRJ gene for a member of the DNAJ protein familyN Seki, A Hattori, A Hayashi, et al.Journal of Human Genetics|May 13, 1999
Isolation and chromosomal assignment of a human gene encoding protein inhibitor of activated STAT3 (PIAS3)N Ueki, N Seki, K Yano, et al.Journal of Human Genetics|May 13, 1999
Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes diseaseA Ogawa, S Yamamoto, M Takayanagi, et al.Journal of Human Genetics|May 13, 1999
Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitutionK Hirata, M Nakagawa, I Higuchi, et al.Journal of Human Genetics|May 13, 1999
A novel nonsense mutation at Glu-631 in a Spanish family with complement component 7 deficiencyT Horiuchi, J M Ferrer, P Serra, et al.Pageof 351