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Gene|June 19, 2001
Identification and localization of two mouse phosphomannomutase genes, Pmm1 and Pmm2L Heykants, E Schollen, S Grünewald, et al.Blood|November 1, 1991
The gene for the alpha 4 subunit of the VLA-4 integrin maps to chromosome 2Q31-32Z H Zhang, S Vekemans, M S Aly, et al.The Journal of Cell Biology|August 1, 1992
Molecular cloning of amphiglycan, a novel integral membrane heparan sulfate proteoglycan expressed by epithelial and fibroblastic cellsG David, B van der Schueren, P Marynen, et al.Bulletin De La Societe Belge D'Ophtalmologie|January 1, 1996
Fundus changes in patients with the mitochondrial DNA point mutation at position 3243C Bonte, A Leys, G Matthijs, et al.The Journal of Biological Chemistry|August 25, 1986
The receptor-binding domain of human alpha 2-macroglobulin. Isolation after limited proteolysis with a bacterial proteinaseF Van Leuven, P Marynen, L Sottrup-Jensen, et al.Prenatal Diagnosis|December 1, 1993
Co-amplification of the cystic fibrosis delta F508 mutation with the HLA DQA1 sequence in single cell PCR: implications for improved assessment of polar bodies and blastomeres in preimplantation diagnosisR Wu, H Cuppens, I Buyse, et al.The Journal of Cell Biology|December 1, 1990
Molecular cloning of a phosphatidylinositol-anchored membrane heparan sulfate proteoglycan from human lung fibroblastsG David, V Lories, B Decock, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
An Algerian child homozygous for the M470V polymorphism and for a deletion of two nucleotides in exon 10 of the CFTR gene, shows severe cystic fibrosis symptomsO Loumi, H Cuppens, R Bakour, et al.Cytogenetic and Genome Research|March 17, 2009
Detection and validation of copy number variation in X-linked mental retardationM Bauters, A Weuts, J Vandewalle, et al.Journal of Medical Genetics|January 1, 1996
Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35)X X Gu, R Decorte, P Marynen, et al.Pageof 28