Showing results (51-60 of 117) with videos related to
Sort By:
Pageof 12
Biochemical and Biophysical Research Communications|November 27, 1985
The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromosome 2L Chan, P VanTuinen, D H Ledbetter, et al.Genomics|October 1, 1989
Multilocus linkage analysis with the human argininosuccinate synthetase geneH Northrup, M Lathrop, S Y Lu, et al.Journal of Medical Genetics|July 1, 1996
Report of a critical recombination further narrowing the TSC1 regionK S Au, J Murrell, A Buckler, et al.Journal of Molecular Evolution|March 1, 1990
Phylogenetic relationships among Tetrahymena species determined using the polymerase chain reactionC F Brunk, R W Kahn, L A SadlerClinical Genetics|September 10, 2004
Genetic analysis of primary microcephaly in Indian families: novel ASPM mutationsA Kumar, S H Blanton, M Babu, et al.Human Genetics|May 1, 1987
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuriaR Chakraborty, A S Lidsky, S P Daiger, et al.Annals of Neurology|June 1, 1988
Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindredH Y Zoghbi, M S Pollack, L A Lyons, et al.Investigative Ophthalmology & Visual Science|December 1, 1994
Cosegregation of codon 807 mutation of the canine rod cGMP phosphodiesterase beta gene and rcd1K Ray, V J Baldwin, G M Acland, et al.American Journal of Human Genetics|February 1, 1989
Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysisH Y Zoghbi, L A Sandkuyl, J Ott, et al.Investigative Ophthalmology & Visual Science|May 1, 2001
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX geneR T Tzekov, Y Liu, M M Sohocki, et al.Pageof 12