ProSobee and fructose intolerance.

Por McInnes, R. R.
Publicado em 1982

The Clinical Psychiatry of Late Life

Por McInnes, R G
Publicado em 1966

Observations on Heredity in Neurosis: (Section of Psychiatry)

Por McInnes, R. G.
Publicado em 1937

Observations on the Relationship between Child and Adult Neurosis

Por McInnes, R. G.
Publicado no Ment Health (Lond) (1943)

Differential diagnosis of cerebral palsy: Lesch-Nyhan syndrome without self-mutilation.

Por Mitchell, G, McInnes, R R
Publicado em 1984

Interallelic complementation in an inborn error of metabolism: genetic heterogeneity in argininosuccinate lyase deficiency.

Por McInnes, R R, Shih, V, Chilton, S
Publicado em 1984

Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidney.

Por Scriver, C R, McInnes, R R, Mohyuddin, F
Publicado em 1975

The Infant Feeding Genogram: a tool for exploring family infant feeding history and identifying support needs

Por Darwent, K. L., McInnes, R. J., Swanson, V.
Publicado no BMC Pregnancy Childbirth (2016)

E. coli host strains significantly affect the quality of small scale plasmid DNA preparations used for sequencing.

Por Taylor, R G, Walker, D C, McInnes, R R
Publicado em 1993

Argininosuccinate lyase deficiency: evidence for heterogeneous structural gene mutations by immunoblotting.

Por Simard, L, O'Brien, W E, McInnes, R R
Publicado em 1986

Cloning and sequence analysis of cDNA for human argininosuccinate lyase.

Por O'Brien, W E, McInnes, R, Kalumuck, K, Adcock, M
Publicado em 1986

Treatment of gyrate atrophy of the choroid and retina with low arginine diet.

Por McInnes, R R, Arshinoff, S A, Bell, L, McCulloch, C
Publicado em 1980

Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chai...

Por Zheng, K, Thorner, P S, Marrano, P, Baumal, R, McInnes, R R
Publicado em 1994

A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defect.

Por Smooker, P M, Christodoulou, J, McInnes, R R, Cotton, R G
Publicado em 1995

Molecular cloning of cDNA for rat argininosuccinate lyase and its expression in rat hepatoma cell lines.

Por Lambert, M A, Simard, L R, Ray, P N, McInnes, R R
Publicado em 1986

Molecular analysis of human argininosuccinate lyase: mutant characterization and alternative splicing of the coding region.

Por Walker, D C, McCloskey, D A, Simard, L R, McInnes, R R
Publicado em 1990

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse.

Por Connell, G, Bascom, R, Molday, L, Reid, D, McInnes, R R, Molday, R S
Publicado em 1991

Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1.

Por Nichols, B. E., Bascom, R., Litt, M., McInnes, R., Sheffield, V. C., Stone, E. M.
Publicado em 1994

Renal disease in carrier female dogs with X-linked hereditary nephritis. Implications for female patients with this disease.

Por Baumal, R., Thorner, P., Valli, V. E., McInnes, R., Marrano, P., Jacobs, R., Binnington, A., Bloedow, A. G.
Publicado em 1991

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.

Por Sohocki, M M, Sullivan, L S, Mintz-Hittner, H A, Birch, D, Heckenlively, J R, Freund, C L, McInnes, R R, Daiger, S P
Publicado em 1998