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Results: 1-9 |
Results: 9
Tensions in implementing the new genetics - Genetic counsellors could be based in genetic centres but be formally linked to general practices
Authors: Donnai, D Kerzin-Storrar, L Craufurd, D Evans, G Clayton-Smith, J Kingston, H
Citation: D. Donnai et al., Tensions in implementing the new genetics - Genetic counsellors could be based in genetic centres but be formally linked to general practices, BR MED J, 321(7255), 2000, pp. 241-241
Genetic registers in clinical practice: a survey of UK clinical geneticists
Authors: Dean, JC Fitzpatrick, DR Farndon, PA Kingston, H Cusine, D
Citation: Jc. Dean et al., Genetic registers in clinical practice: a survey of UK clinical geneticists, J MED GENET, 37(8), 2000, pp. 636-640
Punctate calcification of the epiphyses, visceral malformations, and craniofacial dysmorphism in a female baby
Authors: Slavotinek, A Kingston, H
Citation: A. Slavotinek et H. Kingston, Punctate calcification of the epiphyses, visceral malformations, and craniofacial dysmorphism in a female baby, J MED GENET, 37(10), 2000, pp. 796-798
Familial syndromic esophageal atresia maps to 2p23-p24
Authors: Celli, J van Beusekom, E Hennekam, RCM Gallardo, ME Smeets, DFCM de Cordoba, SR Innis, JW Frydman, M Konig, R Kingston, H Tolmie, J Govaerts, LCP van Bokhoven, H Brunner, HG
Citation: J. Celli et al., Familial syndromic esophageal atresia maps to 2p23-p24, AM J HU GEN, 66(2), 2000, pp. 436-444
Proximal myotonic myopathy (PROMM) presenting as myotonia during pregnancy
Authors: Newman, B Meola, G O'Donovan, DG Schapira, AHV Kingston, H
Citation: B. Newman et al., Proximal myotonic myopathy (PROMM) presenting as myotonia during pregnancy, NEUROMUSC D, 9(3), 1999, pp. 144-149
Two cases with interstitial deletions of chromosome 2 and sex reversal in one
Authors: Slavotinek, A Schwarz, C Getty, JF Stecko, O Goodman, F Kingston, H
Citation: A. Slavotinek et al., Two cases with interstitial deletions of chromosome 2 and sex reversal in one, AM J MED G, 86(1), 1999, pp. 75-81
Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosometelomeres
Authors: Slavotinek, A Rosenberg, M Knight, S Gaunt, L Fergusson, W Killoran, C Clayton-Smith, J Kingston, H Campbell, RHA Flint, J Donnai, D Biesecker, L
Citation: A. Slavotinek et al., Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosometelomeres, J MED GENET, 36(5), 1999, pp. 405-411
A clinical study of type 1 neurofibromatosis in north west England
Authors: McGaughran, JM Harris, DI Donnai, D Teare, D MacLeod, R Westerbeek, R Kingston, H Super, M Harris, R Evans, DGR
Citation: Jm. Mcgaughran et al., A clinical study of type 1 neurofibromatosis in north west England, J MED GENET, 36(3), 1999, pp. 197-203
Feingold syndrome - a cause of profound deafness
Authors: Dodds, A Ramsden, R Kingston, H
Citation: A. Dodds et al., Feingold syndrome - a cause of profound deafness, J LARYNG OT, 113(10), 1999, pp. 919-921
Risultati: 1-9 |