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Journal of Medical Genetics|December 1, 1991
Arginine 109 to glutamine mutation in a girl with ornithine carbamoyl transferase deficiencyS Strautnieks, P Rutland, S Malcolm
Archives of Disease in Childhood|January 1, 1987
The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletionsJ K Cowell, E Thompson, P Rutland
Current Medical Research and Opinion|January 1, 1977
Amitriptyline and weight gain: a biochemical and endocrinological studyB R Nakra, P Rutland, S Verma, et al.
Human Genetics|September 1, 1988
Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastomaJ K Cowell, P Rutland, J Hungerford, et al.
Cancer Genetics and Cytogenetics|July 1, 1987
A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31)J K Cowell, J Hungerford, P Rutland, et al.
Human Genetics|November 1, 1986
Effect of the esterase-D phenotype on its in vitro enzyme activityJ K Cowell, P Rutland, M Jay, et al.
Human Genetics|February 1, 1986
Deletions of the esterase D locus from a survey of 200 retinoblastoma patientsJ K Cowell, P Rutland, M Jay, et al.
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