Showing results (71-80 of 177) with videos related to

Sort By:
Pageof 18
Human Genetics|August 1, 1991
Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyriaJ S Lee, G Lundin, L Lannfelt, et al.
American Journal of Medical Genetics|January 24, 1998
Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic statusT B Wahlin, A Lundin, L Bäckman, et al.
The Journal of General Virology|December 1, 1991
B cell phenotype-dependent expression of the Epstein-Barr virus nuclear antigens EBNA-2 to EBNA-6: studies with somatic cell hybridsB A Contreras-Brodin, M Anvret, S Imreh, et al.
Urological Research|March 26, 1999
Screening for mutations in candidate genes for hypospadiasA Nordenskjöld, E Friedman, M Tapper-Persson, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|November 1, 1991
Evaluation of DNA-based diagnosis for haemophilia AC Wadelius, M Blombäck, P Goonewardena, et al.
The Journal of Biological Chemistry|April 5, 2000
Independent regulation of the myotonic dystrophy 1 locus genes postnatally and during adult skeletal muscle regenerationM Eriksson, T Ansved, L Edstrom, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|November 1, 1993
Genetic carrier detection in Norwegian families with acute intermittent porphyriaE Sagen, A Laegreid, M Anvret, et al.
Clinical Genetics|June 1, 1988
A linkage study of the locus for X-linked Charcot-Marie-Tooth diseaseP Goonewardena, J Welihinda, M Anvret, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 7, 2002
APOE genotypes and disease severity in multiple sclerosisT Masterman, Z Zhang, D Hellgren, et al.
Clinical Genetics|December 1, 1991
Genetic mapping of loci for X-linked retinitis pigmentosaN Dahl, M Sundvall, U Pettersson, et al.
Pageof 18