InsulinMACPHERSON, J. N; FEELY, J.BMJ. British medical journal (International ed.). 1990, Vol 300, Num 6726, pp 731-736, issn 0959-8146Article

Haplotype and AGG-interspersion analysis of FMR1 (CGG)_n alleles in the Danish population : Implications for multiple mutational pathways towards fragile X allelesLARSEN, L. A; ARMSTRONG, J. S. M; GRØNSKOV, K et al.American journal of medical genetics. 2000, Vol 93, Num 2, pp 99-106, issn 0148-7299Article

Population genetics of the fragile-X syndrome : multiallelic model for the FMR1 locusMORTON, N. E; MACPHERSON, J. N.Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 9, pp 4215-4217, issn 0027-8424Article

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the origin of the fragile X syndromeEICHLER, E. E; MACPHERSON, J. N; MURRAY, A et al.Human molecular genetics (Print). 1996, Vol 5, Num 3, pp 319-330, issn 0964-6906Article

Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptionsEICHLER, E. E; HAMMOND, H. A; MACPHERSON, J. N et al.Human molecular genetics (Print). 1995, Vol 4, Num 12, pp 2199-2208, issn 0964-6906Article

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1GUNTER, C; PARADEE, W; SHERMAN, S. L et al.Human molecular genetics (Print). 1998, Vol 7, Num 12, pp 1935-1946, issn 0964-6906Article

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutationMACPHERSON, J. N; BULLMAN, H; YOUINGS, S. A et al.Human molecular genetics (Print). 1994, Vol 3, Num 3, pp 399-405, issn 0964-6906Article

Evolutionary dynamics of the FMR1 locusMORRIS, A; MORTON, N. E; COLLINS, A et al.Annals of human genetics. 1995, Vol 59, pp 283-289, issn 0003-4800, 3Article

Allelic association in the FRAX regionENNIS, S; COLLINS, A; MURRAY, A et al.Annals of human genetics. 2000, Vol 64, pp 513-518, issn 0003-4800, 6Article

Predisposition to the fragile X syndrome in jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotypeFALIK-ZACCAI, T. C; SHACHAK, E; YALON, M et al.American journal of human genetics. 1997, Vol 60, Num 1, pp 103-112, issn 0002-9297Article

The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmissionMURRAY, A; MACPHERSON, J. N; POUND, M. C et al.Human molecular genetics (Print). 1997, Vol 6, Num 2, pp 173-184, issn 0964-6906Article

Extensive linkage disequilibrium in the achaete-scute complex of Drosophila melanogasterMACPHERSON, J. N; WEIR, B. S; BROWN, A. J. L et al.Genetics. 1990, Vol 126, Num 1, pp 121-129, issn 0016-6731, 9 p.Article

Allelic association discriminates draft ordersENNIS, S; COLLINS, A; TAPPER, W et al.Annals of human genetics. 2001, Vol 65, Num 5, pp 503-504, issn 0003-4800Article

Unusual (CGG)_n expansion and recombination in a family with fragile X and DiGeorge syndromeMACPHERSON, J. N; CURTIS, G; CROLLA, J. A et al.Journal of medical genetics. 1995, Vol 32, Num 3, pp 236-239, issn 0022-2593Article

Identification of the FRAXE fragile site in two families ascertained for X linked mental retardationFLYNN, G. A; HIRST, M. C; KNIGHT, S. J. L et al.Journal of medical genetics. 1993, Vol 30, Num 2, pp 97-100, issn 0022-2593Article

Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotypeDENNIS, N. R; CURTIS, G; MACPHERSON, J. N et al.American journal of medical genetics. 1992, Vol 43, Num 1-2, pp 232-236, issn 0148-7299Article

Maternal and larval effects of photoperiod on the induction of larval diapause in two species of fly, Calliphora vicina and Lucilia sericataSAUNDERS, D. S; MACPHERSON, J. N; CAIRNCROSS, K. D et al.Experimental biology. 1986, Vol 46, Num 1, pp 51-58, issn 0176-8638Article