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Discussion on The Mersey Estuary pollution alleviation scheme: Liverpool interceptor sewers by G.N. Olsen, M.F. Danbury and B. LeatherbarrowOLSEN, G. N; DANBURY, M. F; LEATHERBARROW, B et al.Proceedings of the Institution of Civil Engineers. Water, maritime and energy. 2001, Vol 148, Num 4, pp 281-284, issn 0965-0946Article

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disordersBOLTON, Patrick Farrar; DENNIS, N. R; BROWNE, C. E et al.American journal of medical genetics. 2001, Vol 105, Num 8, pp 675-685, issn 0148-7299Article

Linkage of asthma to markers on chromosome 12 in a sample of 240 families using quantitative phenotype scoresWILKINSON, J; GRIMLEY, S; COLLINS, A et al.Genomics (San Diego, Calif.). 1998, Vol 53, Num 3, pp 251-259, issn 0888-7543Article

Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafnessREARDON, W; ROBERTS, S; PHELPS, P. D et al.American journal of medical genetics. 1992, Vol 44, Num 4, pp 513-517, issn 0148-7299Article

Lck is a key target of imatinib and dasatinib in T-cell activationLEE, K. C; OUWEHAND, I; GIANNINI, A. L et al.Leukemia. 2010, Vol 24, Num 4, pp 896-900, issn 0887-6924, 5 p.Article

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypesGRIBBLE, S. M; PRIGMORE, E; SANDSTROM, R et al.Journal of medical genetics. 2005, Vol 42, Num 1, pp 8-16, issn 0022-2593, 9 p.Article

Combination strategies to enhance transdermal permeation of zidovudine (AZT)THOMAS, N. S; PANCHAGNULA, R.Pharmazie. 2003, Vol 58, Num 12, pp 895-898, issn 0031-7144, 4 p.Article

Hardy-Weinberg quality controlGOMES, I; COLLINS, A; LONJOU, C et al.Annals of human genetics. 1999, Vol 63, pp 535-538, issn 0003-4800, 6Article

Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitusMACKAY, D. J. G; HAHNEMANN, J. M. D; CLAYTON-SMITH, J et al.Human genetics. 2006, Vol 119, Num 1-2, pp 179-184, issn 0340-6717, 6 p.Article

Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndromeHOLDEN, S. T; COX, J. J; KESTERTON, I et al.Journal of medical genetics. 2006, Vol 43, Num 9, pp 750-754, issn 0022-2593, 5 p.Article

Candidate gene and mutational analysis in asthma and atopyWILKINSON, J; THOMAS, N. S; MORTON, N et al.International archives of allergy and immunology. 1999, Vol 118, Num 2-4, pp 265-267, issn 1018-2438Conference Paper

Plasmid diversity in ChlamydiaTHOMAS, N. S; LUSHER, M; STOREY, C. C et al.Microbiology (Reading). 1997, Vol 143, pp 1847-1854, issn 1350-0872, 6Article

Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13DENNIS, N. R; VELTMAN, M. W. M; THOMPSON, R et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 5, pp 434-441, issn 1552-4825, 8 p.Article

Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexityROBERTS, S. E; MAGGOUTA, F; THOMAS, N. S et al.American journal of human genetics. 2003, Vol 73, Num 5, pp 1061-1072, issn 0002-9297, 12 p.Article

A study of females with deletions of the short arm of the X chromosomeJAMES, R. S; COPPIN, B; DALTON, P et al.Human genetics. 1998, Vol 102, Num 5, pp 507-516, issn 0340-6717Article

Transmigration of CD34+ cells across specialized and nonspecialized endothelium requires prior activation by growth factors and is mediated by PECAM-1 (CD31)YONG, K. L; WATTS, M; THOMAS, N. S et al.Blood. 1998, Vol 91, Num 4, pp 1196-1205, issn 0006-4971Article

A pseudoautosomal gene in manGOODFELLOW, P. J; DARLING, S. M; THOMAS, N. S et al.Science (Washington, D.C.). 1986, Vol 234, Num 4777, pp 740-743, issn 0036-8075Article

Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypesALDRED, M. A; SANFORD, R. O. C; TREMBATH et al.Journal of medical genetics. 2004, Vol 41, Num 6, pp 433-439, issn 0022-2593, 7 p.Article

Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical regionTHOMAS, N. S; BROWNE, C. E; OLEY, C et al.Human genetics. 1999, Vol 105, Num 5, pp 384-387, issn 0340-6717Article

The glutamine 27 β2-adrenoceptor polymorphism is associated with elevated IgE levels in asthmatic familiesDEWAR, J. C; WILKINSON, J; HALL, I. P et al.Journal of allergy and clinical immunology. 1997, Vol 100, Num 2, pp 261-265, issn 0091-6749Article

The candidate region approach to the genetics of asthma and allergyTHOMAS, N. S; WILKINSON, J; HOLGATE, S. T et al.American journal of respiratory and critical care medicine. 1997, Vol 156, Num 4, pp S144-S151, issn 1073-449X, 2Conference Paper

Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell linesSUTHERS, G. K; HYLAND, V. J; BAKER, E et al.American journal of human genetics. 1990, Vol 47, Num 2, pp 187-195, issn 0002-9297, 9 p.Article

A study of juice analysis by Celite filtration and near infrared polarimetry as an alternative to lead clarificationSNOAD, J. D; THOMAS, N. S.International sugar journal. 2008, Vol 110, Num 1313, issn 0020-8841, 284-290 [6 p.]Article

A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletionsLACHLAN, K. L; YOUINGS, S; COSTA, T et al.Human genetics. 2006, Vol 118, Num 5, pp 640-651, issn 0340-6717, 12 p.Article

Linkage analysis of the 5q31-33 candidate region for asthma in 240 UK familiesHOLLOWAY, J. W; LONJOU, C; HOLGATE, S. T et al.Genes and immunity. 2001, Vol 2, Num 1, pp 20-24, issn 1466-4879, 5 p.Article

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