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Results:
1-10
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Results: 10
Authors:
McKee, SA
Barnicoat, A
Fryer, A
Flinter, F
McCormick, D
McKeown, C
Citation: Sa. Mckee et al., Joint and skin laxity with Dandy-Walker malformation and contractures: a distinct recessive syndrome?, CLIN DYSMOR, 10(3), 2001, pp. 177-180
Authors:
de Vries, BBA
White, SM
Knight, SJL
Regan, R
Homfray, T
Young, ID
Super, M
McKeown, C
Splitt, M
Quarrell, OWJ
Trainer, AH
Niermeijer, MF
Malcolm, S
Flint, J
Hurst, JA
Winter, RM
Citation: Bba. De Vries et al., Clinical studies on submicroscopic subtelomeric rearrangements: a checklist, J MED GENET, 38(3), 2001, pp. 145-150
Authors:
Bulman, MP
Kusumi, K
Frayling, TM
McKeown, C
Garrett, C
Lander, ES
Krumlauf, R
Hattersley, AT
Ellard, S
Turnpenny, PD
Citation: Mp. Bulman et al., Mutations in the human Delta homologue, DLL3, cause axial skeletal defectsin spondylocostal dysostosis, NAT GENET, 24(4), 2000, pp. 438-441
Authors:
Perveen, R
Lloyd, IC
Clayton-Smith, J
Churchill, A
van Heyningen, V
Hanson, I
Taylor, D
McKeown, C
Super, M
Kerr, B
Winter, R
Black, GCM
Citation: R. Perveen et al., Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations, INV OPHTH V, 41(9), 2000, pp. 2456-2460
Authors:
Hagan, DM
Ross, AJ
Strachan, T
Lynch, SA
Ruiz-Perez, V
Wang, YM
Scambler, P
Custard, E
Reardon, W
Hassan, S
Muenke, M
Nixon, P
Papapetrou, C
Winter, RM
Edwards, Y
Morrison, K
Barrow, M
Cordier-Alex, MP
Correia, P
Galvin-Parton, PA
Gaskill, S
Gaskin, KJ
Garcia-Minaur, S
Gereige, R
Hayward, R
Homfray, T
McKeown, C
Murday, V
Plauchu, H
Shannon, N
Spitz, L
Lindsay, S
Citation: Dm. Hagan et al., Mutation analysis and embryonic expression of the HLXB9 Currarino syndromegene, AM J HU GEN, 66(5), 2000, pp. 1504-1515
Authors:
Richards, FM
McKee, SA
Rajpar, MH
Cole, TRP
Evans, DGR
Jankowski, JA
McKeown, C
Sanders, DSA
Maher, ER
Citation: Fm. Richards et al., Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancer, HUM MOL GEN, 8(4), 1999, pp. 607-610
Authors:
Wang, ZJ
Churchman, M
Avizienyte, E
McKeown, C
Davies, S
Evans, DGR
Ferguson, A
Ellis, I
Xu, WH
Yan, ZY
Aaltonen, LA
Tomlinson, IPM
Citation: Zj. Wang et al., Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients, J MED GENET, 36(5), 1999, pp. 365-368
Authors:
McKeown, C
Haszeldine, RS
Couples, GD
Citation: C. Mckeown et al., Mathematical modelling of groundwater flow at Sellafield, UK, ENG GEOL, 52(3-4), 1999, pp. 231-250
Authors:
Pulleyn, LJ
Winter, RM
Reardon, W
McKeown, C
Jones, B
Hayward, R
Evans, R
Malcolm, S
Citation: Lj. Pulleyn et al., Further evidence from two families that craniofrontonasal dysplasia maps to Xp22, CLIN GENET, 55(6), 1999, pp. 473-477
Authors:
Burn, J
Alonso, A
Bertario, L
Bishop, T
Bisgaard, ML
Cummings, J
Davidson, R
Delhanty, J
Demant, P
Dunlop, M
Eccles, D
Ellis, A
Evans, G
Fidalgo, P
Fodde, R
Haites, N
Hodgson, S
Hultcrantz, R
Huson, S
Jarvinen, H
Kartheuser, A
Kleibeuker, J
Lenaerts, C
Lucasson, A
Lunt, P
McDermot, K
McKay, J
McKeown, C
Maher, E
Mathers, J
Mecklin, JP
Moslein, G
Murday, V
Nagengast, F
Northover, JMA
Obrador, A
Parks, TG
Paraskeva, C
Phillips, R
San Roman, C
Ruscheoff, J
Sampson, J
Shepherd, N
Tempesta, A
Trembath, R
Turnpenny, P
Vasen, HFA
Citation: J. Burn et al., Concerted action polyp prevention, CAPP2: A trial of aspirin and/or resistant starch in people at risk of hereditary non-polyposis colon cancer (HNPCC), BIOM HLTH R, 24, 1998, pp. 17-23
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