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Results:
1-21
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Results: 21
Authors:
Dean, G
Nevin, NC
Mikkelsen, M
Karadima, G
Petersen, MB
Kelly, M
O'Sullivan, J
Citation: G. Dean et al., Investigation of a cluster of children with Down Syndrome born to mothers who had attended a school in Dundalk, Ireland. (vol 57, pg 793, 2000), OCC ENVIR M, 58(5), 2001, pp. 353-353
Authors:
Nevin, NC
Citation: Nc. Nevin, Future direction of medical genetics, ULSTER MED, 70(1), 2001, pp. 1-2
Authors:
Hughes, J
Nevin, NC
Morrison, PJ
Citation: J. Hughes et al., Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene, ULSTER MED, 70(1), 2001, pp. 47-50
Authors:
Calvert, JT
Burns, S
Riney, TJ
Sahoo, T
Orlow, SJ
Nevin, NC
Haisley-Royster, C
Prose, N
Simpson, SA
Speer, MC
Marchuk, DA
Citation: Jt. Calvert et al., Additional glomangioma families link to chromosome 1p: No evidence for genetic heterogeneity, HUMAN HERED, 51(3), 2001, pp. 180-182
Authors:
Nevin, NC
Spink, J
Citation: Nc. Nevin et J. Spink, Recommendations proposed for adenovirus gene therapy trials in the UK, MOL MED TOD, 6(12), 2000, pp. 461-461
Authors:
Dean, G
Nevin, NC
Mikkelsen, M
Karadima, G
Petersen, MB
Kelly, M
O'Sullivan, J
Citation: G. Dean et al., Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland, OCC ENVIR M, 57(12), 2000, pp. 793-804
Authors:
Nevin, NC
Citation: Nc. Nevin, What has happened to gene therapy?, EUR J PED, 159, 2000, pp. S240-S242
Authors:
Bhat, M
Morrison, PJ
Getty, A
McManus, D
Tubman, R
Nevin, NC
Citation: M. Bhat et al., First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH, AM J MED G, 91(3), 2000, pp. 201-203
Authors:
Greeves, LG
Patterson, CC
Carson, DJ
Thom, R
Wolfenden, MC
Zschocke, J
Graham, CA
Nevin, NC
Trimble, ER
Citation: Lg. Greeves et al., Effect of genotype on changes in intelligence quotient after dietary relaxation in phenylketonuria and hyperphenylalaninaemia, ARCH DIS CH, 82(3), 2000, pp. 216-221
Authors:
Denison, CK
Barnes, R
Gibson, B
Hunt, A
Hart, I
Steel, M
Casimir, C
Liu, D
Nevin, NC
Anionwu, E
Burn, J
Dayan, A
Denison, K
Johnston, P
Marteau, T
Neil, J
Pinching, A
Platt, E
Richards, B
Steel, CM
Train, I
Citation: Ck. Denison et al., Gene Therapy Advisory Committee - Report on the potential use of gene therapy in utero, HUM GENE TH, 10(4), 1999, pp. 689-692
Authors:
Calvert, JT
Riney, TJ
Kontos, CD
Cha, EH
Prieto, VG
Shea, CR
Berg, JN
Nevin, NC
Simpson, SA
Pasyk, KA
Speer, MC
Peters, KG
Marchuk, DA
Citation: Jt. Calvert et al., Allelic and locus heterogeneity in inherited venous malformations, HUM MOL GEN, 8(7), 1999, pp. 1279-1289
Authors:
Morrison, PJ
Nevin, NC
Citation: Pj. Morrison et Nc. Nevin, Cancer genetics services in Northern Ireland, DIS MARKER, 15(1-3), 1999, pp. 37-40
Authors:
Morrison, PJ
Chu, CE
Nevin, NC
Citation: Pj. Morrison et al., A second family with probable CRAC (colorectal adenomata and carcinoma) syndrome - A new familial cancer, DIS MARKER, 15(1-3), 1999, pp. 120-122
Authors:
Morrison, PJ
Steel, CM
Vasen, HFA
Eccles, D
Evans, DGR
Moller, P
Hodgson, S
Stoppa-Lyonnet, D
Chang-Claude, J
Caligo, M
Olah, E
Haites, NE
Nevin, NC
Citation: Pj. Morrison et al., Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe, DIS MARKER, 15(1-3), 1999, pp. 159-165
Authors:
Moller, P
Evans, G
Haites, N
Vasen, H
Reis, MM
Anderson, E
Apold, J
Hodgson, S
Eccles, D
Olsson, H
Stoppa-Lyonnet, D
Chang-Claude, J
Morrison, PJ
Bevilacqua, G
Heimdal, K
Maehle, L
Lalloo, F
Gregory, H
Preece, P
Borg, A
Nevin, NC
Caligo, M
Steel, CM
Citation: P. Moller et al., Guidelines for follow-up of women at high risk for inherited breast cancer: Consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer, DIS MARKER, 15(1-3), 1999, pp. 207-211
Authors:
Nevin, NC
Leonard, AG
Jones, B
Citation: Nc. Nevin et al., Frontonasal dysostosis in two successive generations, AM J MED G, 87(3), 1999, pp. 251-253
Authors:
Nevin, NC
Thomas, PS
Davis, RI
Cowie, GH
Citation: Nc. Nevin et al., Melorheostosis in a family with autosomal dominant osteopoikilosis, AM J MED G, 82(5), 1999, pp. 409-414
Authors:
Asghar, M
Nevin, NC
Beattie, ED
McManus, D
Roberts, GMA
Phillips, JA
Citation: M. Asghar et al., Contiguous gene deletion syndrome involving glycerol kinase and Duchenne muscular dystrophy loci, J INH MET D, 22(8), 1999, pp. 933-935
Authors:
McNicholl, F
McMullin, MF
Nevin, NC
McMillan, C
Citation: F. Mcnicholl et al., Hereditary benign telangiectasia - first family in Northern Ireland, ULSTER MED, 68(2), 1999, pp. 106-107
Authors:
Nevin, NC
Citation: Nc. Nevin, Future of gene therapy, HOSP MED, 59(12), 1998, pp. 977-977
Authors:
Covello, SP
Irvine, AD
McKenna, KE
Munro, CS
Nevin, NC
Smith, FJD
Uitto, J
McLean, WHI
Citation: Sp. Covello et al., Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland, J INVES DER, 111(6), 1998, pp. 1207-1209
Risultati:
1-21
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