The physical mapping of the mouse genomeBROWN, S. D. M.Techniques in the behavioral and neural sciences. 1992, Vol 8, pp 215-228, issn 0921-0709Article

The mouse genome project and human genetics. A report from the 5th international mouse genome mapping workshop, Lunteren, HollandBROWN, S. D. M.Genomics (San Diego, Calif.). 1992, Vol 13, Num 2, pp 490-492, issn 0888-7543Article

ENU mutagenesis and the search for deafness genesHARDISTY, R. E; MBURU, P; BROWN, S. D. M et al.British journal of audiology. 1999, Vol 33, Num 5, pp 279-283, issn 0300-5364Conference Paper

Xist expression from an Xist YAC transgene carried on the mouse Y chromosomeMATSUURA, S; EPISKOPOU, V; HAMVAS, R et al.Human molecular genetics (Print). 1996, Vol 5, Num 4, pp 451-459, issn 0964-6906Article

Genetic mapping of a gene encoding an atypical protein kinase C, protein kinase C lambda, to the proximal region of mouse chromosome 3QUADERI, N. A; GIANFRANCESCO, F; BROWN, S. D. M et al.Genomics (San Diego, Calif.). 1995, Vol 29, Num 3, pp 815-816, issn 0888-7543Article

Genes and deafnessSTEEL, K. P; BROWN, S. D. M.Trends in genetics (Regular ed.). 1994, Vol 10, Num 12, pp 428-435, issn 0168-9525Article

Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type IEVANS, K. L; FANTES, J; ST. CLAIR, D et al.Human molecular genetics (Print). 1993, Vol 2, Num 2, pp 115-118, issn 0964-6906Article

Co-amplification of L1 line elements with localised low copy repeats in Giemsa dark bands : implications for genome organisationNASIR, J; MACONOCHIE, M. K; BROWN, S. D. M et al.Nucleic acids research. 1991, Vol 19, Num 12, pp 3255-3260, issn 0305-1048, 6 p.Article

The multipoint genetic mapping of mouse chromosome 16IRVING, N. G; HARDY, J. A; BROWN, S. D. M et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 2, pp 386-389, issn 0888-7543, 4 p.Article

Microdissection of and microcloning from the short arm of human chromosome 2BATES, G. P; WAINWRIGHT, B. J; WILLIAMSON, R et al.Molecular and cellular biology (Print). 1986, Vol 6, Num 11, pp 3826-3830, issn 0270-7306Article

Resonant Raman scattering characterization of carbon nanotubes grown with different catalystsCORIO, P; TEMPERINI, M. L. A; LEITE, C. F et al.Chemical physics letters. 2001, Vol 350, Num 5-6, pp 373-380, issn 0009-2614Article

Towards new models of disease and physiology in the neurosciences: the role of induced and naturally occurring mutationsHUNTER, A. J; NOLAN, P. M; BROWN, S. D. M et al.Human molecular genetics (Print). 2000, Vol 9, Num 6, pp 893-900, issn 0964-6906Article

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing lossLIU, X.-Z; XIA JUAN XIA; LI RONG XU et al.Human molecular genetics (Print). 2000, Vol 9, Num 1, pp 63-67, issn 0964-6906Article

In-situ Raman study on electrochemical Li insertion into polyparaphenylene-based disordered carbonENDO, M; KIM, C; KARAKI, T et al.Carbon (New York, NY). 1998, Vol 36, Num 9, pp 1403-1406, issn 0008-6223Article

Li storage behavior in polyparaphenylene(PPP)-based disordered carbon as a negative electrode for Li ion batteriesENDO, M; KIM, C; HIRAOKA, T et al.Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals. 1998, Vol 310, pp 353-358, issn 1058-725XConference Paper

Combining mutagenesis and genomics in the mouse - closing the phenotype gapBROWN, S. D. M; PETERS, J.Trends in genetics (Regular ed.). 1996, Vol 12, Num 11, pp 433-435, issn 0168-9525Article

Analysis of the Pax-3 gene in the mouse mutant splotchGOULDING, M; STERRER, S; FLEMING, J et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 2, pp 355-363, issn 0888-7543Article

The α2 chain of type 1 collagen does not map to mouse chromosome 16 but maps close to the Met proto-oncogene on mouse chromosome 6IRVING, N. G; HARDY, J. A; BAHARY, N et al.Cytogenetics and cell genetics. 1989, Vol 50, Num 2-3, pp 121-122, issn 0301-0171Article

Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crossesBROCKDORFF, N; FISHER, E. M. C; CAVANNA, J. S et al.EMBO journal (Print). 1987, Vol 6, Num 11, pp 3291-3297, issn 0261-4189Article

Mouse mutagenesis: systematic studies of mammalian gene functionBROWN, S. D. M; NOLAN, P. M.Human molecular genetics (Print). 1998, Vol 7, Num 10, pp 1627-1633, issn 0964-6906Article

Myosin VIIA gene : heterogeneity of the mutations responsible for Usher syndrome type IBLEVY, G; LEVI-ACOBAS, F; MUNNICH, A et al.Human molecular genetics (Print). 1997, Vol 6, Num 1, pp 111-116, issn 0964-6906Article

Genetic mapping of the mouse neuromuscular mutation kyphoscoliosisSKYNNER, M. J; GANGADHARAN, U; COULTON, G. R et al.Genomics (San Diego, Calif.). 1995, Vol 25, Num 1, pp 207-213, issn 0888-7543Article

Genetic deafness-progress with mouse modelsBROWN, S. D. M; STEEL, K. P.Human molecular genetics (Print). 1994, Vol 3, pp 1453-1456, issn 0964-6906, REVIEWArticle

Linkage analysis of the whirler deafness gene on mouse chromosome 4FLEMING, J; ROGERS, M. J. C; BROWN, S. D. M et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 1, pp 42-48, issn 0888-7543Article

The search for the mouse X-chromosome inactivation centreRASTAN, S; BROWN, S. D. M.Genetical research. 1990, Vol 56, Num 2-3, pp 99-106, issn 0016-6723, 8 p.Article