Showing results (151-160 of 232) with videos related to
Sort By:
Pageof 24
Human Mutation|January 1, 1997
Familial ligand-defective apolipoprotein B-100: simultaneous detection of the ARG3500-->GLN and ARG3531-->CYS mutations in a French populationJ P Rabès, M Varret, B Saint-Jore, et al.Cancer Research|June 15, 1993
Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approachE Austruy, M Cohen-Salmon, C Antignac, et al.Annals of the New York Academy of Sciences|January 1, 1985
Isolation and characterization of the human fibrillar collagen genesF Ramirez, M Bernard, M L Chu, et al.Circulation|December 1, 1994
Correlation between decreased myocardial glucose phosphorylation and the DNA mutation size in myotonic dystrophyD Annane, D Duboc, B Mazoyer, et al.Human Molecular Genetics|July 21, 1998
Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacitiesA S Lia, H Seznec, H Hofmann-Radvanyi, et al.Journal of Medical Genetics|February 1, 1992
A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium studyM Sarfarazi, P Tsipouras, R Del Mastro, et al.Annales De Genetique|January 1, 1997
PEG1 expression in maternal uniparental disomy 7L Cuisset, C Le Stunff, J M Dupont, et al.Annales De Genetique|January 1, 1984
The structural gene for transferrin (TF) maps to 3q21----3qterC Huerre, G Uzan, K H Grzeschik, et al.Tissue Antigens|October 18, 2000
HLA-DRB1 and DQB1 genotypes in patients with insulin-dependent neonatal diabetes mellitus. A study of 13 casesE Marquis, I Le Monnier de Gouville, C Bouvattier, et al.European Journal of Human Genetics : EJHG|January 1, 1993
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization eventI Henry, A Puech, A Riesewijk, et al.Pageof 24