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Journal of Medical Genetics|August 1, 1997
Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1K A Brown, L I al-Gazali, L M Moynihan, et al.Nucleic Acids Research|March 11, 1993
The production of PCR products with 5' single-stranded tails using primers that incorporate novel phosphoramidite intermediatesC R Newton, D Holland, L E Heptinstall, et al.Biochemical and Biophysical Research Communications|March 6, 1997
Mapping the minimal domain of hMSH-2 sufficient for binding mismatched oligonucleotidesA Whitehouse, J Deeble, G R Taylor, et al.The British Journal of Ophthalmology|June 30, 2000
Genetic screening in a large family with juvenile onset primary open angle glaucomaA P Booth, R Anwar, H Chen, et al.Nature|November 5, 1984
Isolation of cDNA clones encoding the 20K T3 glycoprotein of human T-cell receptor complexP van den Elsen, B A Shepley, J Borst, et al.International Journal of Cancer|December 15, 1994
The common molecular genetic alterations in Dukes' B and C colorectal carcinomas are not short-term prognostic indicators of survivalB R Dix, P Robbins, R Soong, et al.Public Health Reports (Washington, D.C. : 1974)|January 1, 1990
State level expert review committees--are they protected?R F Wright, J C SmithProteins|March 28, 1998
Structural modeling of the complex between an acetylcholine receptor-mimicking antibody and its snake toxin antigenC Tenette-Souaille, J C SmithDevelopmental Biology|July 1, 1983
The origin of the mesoderm in an anuran, Xenopus laevis, and a urodele, Ambystoma mexicanumJ C Smith, G M MalacinskiPageof 176