Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiencyBROOKS-WILSON, A; MARCIL, M; LOUBSER, O et al.Nature genetics. 1999, Vol 22, Num 4, pp 336-345, issn 1061-4036Article

Structure-function relationships in cellular and viral fps/fes cytoplasmic protein-tyrosine kinasesPAWSON, T; GREER, P; MORAN, M et al.Advances in experimental medicine and biology. 1988, Vol 234, pp 55-64, issn 0065-2598Conference Paper

Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol effluxMARCIL, M; BROOKS-WILSON, A; OUELLETTE, B. F. F et al.Lancet (British edition). 1999, Vol 354, Num 9187, pp 1341-1346, issn 0140-6736Article

The myristylation signal of p60^v-src functionally complements the N-terminal fps-specific region of P130^gag-fpsBROOKS-WILSON, A. R; BALL, E; PAWSON, T et al.Molecular and cellular biology (Print). 1989, Vol 9, Num 5, pp 2214-2219, issn 0270-7306, 6 p.Article

A cluster of CpG islands at D10S94, near the locus responsible for multiplke endocrine neoplasia type 2A (MEN2A)BROOKS-WILSON, A. R; SMAILUS, D. E; GOODFELLOW, P. J et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 2, pp 339-343, issn 0888-7543Article

Isolation of DNA fragments from A human chromosomal subregion by Alu PCR differential hybridizationBERNARD, L. E; BROOKS-WILSON, A. R; WOOD, S et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 2, pp 241-246, issn 0888-7543, 6 p.Article

Additional RFLPs at D10S94 and the development of PCR-based variant detection systems : implications for disease genotype prediction in MEN 2A, MEN 2B, and MTC1 familiesBROOKS-WILSON, A. R; SMAILUS, D; GILCHRIST, D et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 1, pp 233-234, issn 0888-7543Article

Human repeat element-mediated PCR : cloning and mapping of chromosome 10 DNA markersBROOKS-WILSON, A. R; SMAILUS, D. E; WEIER, H.-U. G et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 2, pp 409-414, issn 0888-7543Article

Genomic and yeast artificial chromosome long-range physical maps linking six loci in 10q11.2 and spanning the multiple endocrine neoplasia type 2A (MEN2A) regionBROOKS-WILSON, A. R; LICHTER, J. B; WARD, D. C et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 3, pp 611-617, issn 0888-7543Article

A new DNA marker (D10S94) very tightly linked to the multiple endocrine neoplasia 2A (MEN2A) locusGOODFELLOW, P. J; MYERS, S; ANDERSON, L. L et al.American journal of human genetics. 1990, Vol 47, Num 6, pp 952-956, issn 0002-9297Article

A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locusLICHTER, J. B; JINGSHI WU; BROOKS-WILSON, A. R et al.Human genetics. 1993, Vol 90, Num 5, pp 516-520, issn 0340-6717Article

BCL2 mutations in diffuse large B-cell lymphomaSCHUETZ, J. M; JOHNSON, N. A; BROOKS-WILSON, A. R et al.Leukemia. 2012, Vol 26, Num 6, pp 1383-1390, issn 0887-6924, 8 p.Article

Germline E-cadherin mutations in hereditary disuse gastric cancer: assessment of 42 new families and review of genetic screening criteriaBROOKS-WILSON, A. R; KAURAH, P; KELSEY, M et al.Journal of medical genetics. 2004, Vol 41, Num 7, pp 508-517, issn 0022-2593, 10 p.Article