Heterogeneity of phenylketonuria at the clinical, protein and DNA levelsCOTTON, R. G. H.Journal of inherited metabolic disease. 1990, Vol 13, Num 5, pp 739-750, issn 0141-8955, 12 p.Article

Detection of single base changes in nucleic acidsCOTTON, R. G. H.Biochemical journal (London. 1906). 1989, Vol 263, Num 1, pp 1-10, issn 0006-2936, 10 p.Article

A model for hyperphenylalaninaemia due to tetrahydrobiopterin deficiencyCOTTON, R. G. H.Journal of inherited metabolic disease. 1986, Vol 9, Num 1, pp 4-14, issn 0141-8955Article

Monoclonal antibodies in the study of structure-fonction relationships of proteinsCOTTON, R. G. H.Medicinal research reviews (Print). 1985, Vol 5, Num 1, pp 77-106, issn 0198-6325Article

Current methods of mutation detectionCOTTON, R. G. H.Mutation research. 1993, Vol 285, Num 1, pp 125-144, issn 0027-5107Article

Slowly but surely towards better scanning for mutationsCOTTON, R. G. H.Trends in genetics (Regular ed.). 1997, Vol 13, Num 2, pp 43-46, issn 0168-9525Article

Chemical reactivity of matched cytosine and thymine bases near mismatched and unmatched bases in a heteroduplex between DNA strands with multiple differencesCOTTON, R. G. H; CAMPBELL, R. D.Nucleic acids research. 1989, Vol 17, Num 11, pp 4223-4233, issn 0305-1048Article

The response of embryonal carcinoma cells to retinoic acid depends on colony sizeKOOPMAN, P; COTTON, R. G. H.Differentiation (London). 1986, Vol 31, Num 1, pp 55-60, issn 0301-4681Article

Detection of 81 of 81 known mouse β-globin promoter mutations with T4 endonuclease VII : The EMC methodYOUIL, R; KEMPER, B; COTTON, R. G. H et al.Genomics (San Diego, Calif.). 1996, Vol 32, Num 3, pp 431-435, issn 0888-7543Article

³⁵S-labelled probes improve detection of mismatched base pairs by chemical cleavageSALEEBA, J. A; COTTON, R. G. H.Nucleic acids research. 1991, Vol 19, Num 7, issn 0305-1048, p. 1712Article

Methods of detection of single base substitutions in clinical genetic practiceFORREST, S; COTTON, R. G. H.Molecular biology & medicine. 1990, Vol 7, Num 5, pp 451-459, issn 0735-1313, 9 p.Article

Pluripotent differentiation of single F9 embryonal carcinoma cellsKOOPMAN, P; COTTON, R. G. H.Experimental cell research. 1987, Vol 168, Num 2, pp 567-571, issn 0014-4827Article

Single-tube chemical cleavage of mismatch : Successive treatment with hydroxylamine and osmium tetroxideRAMUS, S. J; COTTON, R. G. H.BioTechniques. 1996, Vol 21, Num 2, pp 216-220, issn 0736-6205, 3 p.Article

Mutation detectionCOTTON, R. G. H; MALCOLM, A. D. B.Nature (London). 1991, Vol 353, Num 6344, pp 582-583, issn 0028-0836Article

A factor produced by feeder cells which inhibits embryonal carcinoma cell differentiation: characterization and partial purificationKOOPMAN, P; COTTON, R. G. H.Experimental cell research. 1984, Vol 154, Num 1, pp 233-242, issn 0014-4827Article

Polymorphism in the 3' untranslated region of the phenylalanine hydroxylase gene detected by enzyme mismatch cleavage : evolution of haplotypesRAMUS, S. J; COTTON, R. G. H.Human genetics. 1995, Vol 96, Num 6, pp 741-743, issn 0340-6717Article

Rapid chemical mapping of dengue virus variability using RNA isolated directly from cellsCOTTON, R. G. H; WRIGHT, P. J.Journal of virological methods. 1989, Vol 26, Num 1, pp 67-76, issn 0166-0934, 10 p.Article

The role of phospholipases A2 in schizophreniaLAW, M. H; COTTON, R. G. H; BERGER, G. E et al.Molecular psychiatry. 2006, Vol 11, Num 6, pp 547-556, issn 1359-4184, 10 p.Article

Identification and in vitro expression of mutations causing dihydropteridine reductase deficiencySMOOKER, P. M; HOWELLS, D. W; COTTON, R. G. H et al.Biochemistry (Easton). 1993, Vol 32, Num 25, pp 6443-6449, issn 0006-2960Article

Prenatal diagnosis of DHPR deficiency by direct detection of mutationSMOOKER, P. M; COTTON, R. G. H; LIPSON, A et al.Prenatal diagnosis. 1993, Vol 13, Num 9, pp 881-884, issn 0197-3851Article

Use of the chemical cleavage of mismatch method for prenatal diagnosis of alpha-1-antitrypsin deficiencyFORREST, S. M; DRY, P. J; COTTON, R. G. H et al.Prenatal diagnosis. 1992, Vol 12, Num 2, pp 133-137, issn 0197-3851Article

A spontaneous mutation causing unstable Hb Hammersmith : detection of the β42 TTT→TCT change by CCM and direct sequencingDIANZANI, I; RAMUS, S; COTTON, R. G. H et al.British journal of haematology. 1991, Vol 79, Num 1, pp 127-129, issn 0007-1048Article

Liver enzyme activites in hyperphenylalaninaemia due to a defective synthesis of tetrahydrobiopterinDHONDT, J.-L; COTTON, R. G. H; DANKS, D. M et al.Journal of inherited metabolic disease. 1985, Vol 8, Num 2, pp 47-48, issn 0141-8955Article

Delineation of the catalytic core of phenylalanine hydroxylase and identification of glutamate 286 as a critical residue for pterin functionDICKSON, P. W; JENNINGS, I. G; COTTON, R. G. H et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 32, pp 20369-20375, issn 0021-9258Article

The use of resolvases T4 endonuclease VII and T7 endonuclease I in mutation detectionBABON, J. J; MCKENZIE, M; COTTON, R. G. H et al.Molecular biotechnology. 2003, Vol 23, Num 1, pp 73-81, issn 1073-6085, 9 p.Article