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The Journal of Biological Chemistry|July 5, 1991
Cloning, primary sequence, and chromosomal mapping of a human flavin-containing monooxygenase (FMO1)C Dolphin, E A Shephard, S Povey, et al.Lancet (London, England)|July 25, 2000
Non-penetrance in tuberous sclerosisJ P Osborne, A C Jones, M W Burley, et al.Lancet (London, England)|March 21, 1987
Evidence that the gene for tuberous sclerosis is on chromosome 9A E Fryer, A Chalmers, J M Connor, et al.Journal of the National Cancer Institute|October 1, 1985
Characteristics of four new human cell lines derived from squamous cell carcinomas of the head and neckH T Rupniak, C Rowlatt, E B Lane, et al.Annals of Human Genetics|May 1, 1990
The assignment of the genes coding for human complement components C6 and C7 to chromosome 5S J Jeremiah, C M Abbott, Z Murad, et al.Annals of Human Genetics|October 1, 1994
Evaluation of a transgenic mouse model for alpha-1-antitrypsin (AAT) related liver diseaseR Ali, S Perfumo, C della Rocca, et al.International Journal of Cancer|August 19, 1991
Characterization of the new bladder cancer cell line HOK-1: expression of transitional, squamous and glandular differentiation patternsF A Offner, G Ott, S Povey, et al.Annals of Human Genetics|May 1, 1994
Two loci for tuberous sclerosis: one on 9q34 and one on 16p13S Povey, M W Burley, J Attwood, et al.The Journal of Clinical Investigation|October 6, 1997
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) geneL J Bruce, D L Cope, G K Jones, et al.Annals of Human Genetics|March 30, 2000
Report and abstracts of the Sixth International Workshop on chromosome 9B P Chadwick, L J Campbell, C L Jackson, et al.Pageof 20