Showing results (221-230 of 244) with videos related to
Sort By:
Pageof 25
Nucleic Acids Research|July 22, 1998
Characterization of whole genome radiation hybrid mapping resources for non-mammalian vertebratesC Kwok, R M Korn, M E Davis, et al.Nature|December 8, 1994
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related geneJ W Foster, M A Dominguez-Steglich, S Guioli, et al.Genome Research|January 24, 1998
A first-generation whole genome-radiation hybrid map spanning the mouse genomeL C McCarthy, J Terrett, M E Davis, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 29, 1995
The role of SOX9 in autosomal sex reversal and campomelic dysplasiaA J Schafer, M A Dominguez-Steglich, S Guioli, et al.Neurogenetics|May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screenF Coraddu, S Sawcer, R Feakes, et al.Vox Sanguinis|February 1, 1980
The rare phenotype En(a-) in a French-Canadian familyV Taliano, R M Guévin, D Hébert, et al.Vox Sanguinis|January 1, 1993
Quantitation of D sites on selected 'weak D' and 'partial D' red cellsB Gorick, D C McDougall, W H Ouwehand, et al.Annals of Human Genetics|July 1, 1981
Deficiency of malic enzyme: a possible marker for malignancy in lymphoid cellsS Povey, S Jeremiah, E Arthur, et al.Human Genetics|January 1, 1983
Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophyM Sarfarazi, P S Harper, H M Kingston, et al.Journal of Neuroimmunology|September 25, 1999
No evidence for association of multiple sclerosis with the complement factors C6 and C7J Chataway, S Sawcer, D Sherman, et al.Pageof 25