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Human Mutation|October 3, 2000
Oligonucleotide microarray based detection of repetitive sequence changesJ G Hacia, K Edgemon, N Fang, et al.Genomics|May 15, 1994
Localization of the gene for ATP citrate lyase (ACLY) distal to gastrin(GAS) and proximal to D17S856 on chromosome 17q12-q21F J Couch, K J Abel, L C Brody, et al.Human Genetics|December 1, 1993
An EcoRI RFLP in the 5' region of the human NF1 geneE Reyniers, K De Boulle, D A Marchuk, et al.American Journal of Human Genetics|April 1, 1991
Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr)M C Iannuzzi, N Hidaka, M Boehnke, et al.Gastroenterology|December 1, 1993
Localization of the cystic fibrosis transmembrane conductance regulator in human bile duct epithelial cellsJ A Cohn, T V Strong, M R Picciotto, et al.Human Molecular Genetics|November 1, 1995
The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different speciesK Savitsky, S Sfez, D A Tagle, et al.Proceedings of the National Academy of Sciences of the United States of America|March 4, 1997
The ataxia-telangiectasia gene product, a constitutively expressed nuclear protein that is not up-regulated following genome damageK D Brown, Y Ziv, S N Sadanandan, et al.Clinical Biochemistry|October 1, 1990
Phenotypic and molecular biological analysis of human butyrylcholinesterase variantsB N La Du, C F Bartels, C P Nogueira, et al.Nucleic Acids Research|September 25, 1999
Design of modified oligodeoxyribonucleotide probes to detect telomere repeat sequences in FISH assaysJ G Hacia, E A Novotny, R A Mayer, et al.Nature Genetics|October 1, 1995
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsJ P Struewing, D Abeliovich, T Peretz, et al.Pageof 24