Zobrazeno 1 - 10
of 81
pro vyhledávání: '"M. Leversha"'
Autor:
PB Sinclair, Anthony R. Green, Alistair Reid, M Leversha, EP Nacheva, Brian J. P. Huntly, Kim Champion, J. Chang, Nick Telford, A Bench
Publikováno v:
Blood. 95:738-743
The hallmark of chronic myeloid leukemia (CML) is the BCR-ABL fusion gene, which is usually formed as a result of the t(9;22) translocation. Patients with CML show considerable heterogeneity both in their presenting clinical features and in the time
Publikováno v:
Journal of Medical Genetics. 32:301-305
We report an infant with pre- and postnatal microcephaly and growth retardation, a distinctive face, and developmental delay. The initial diagnosis was of Seckel syndrome. He became pancytopenic at 16 months and died soon after. His bone marrow was o
Autor:
AJ COFFEY, RA BROOKSBANK, O. BRANDAU, T. OOHASAI, GR HOWELL, JM BYE, AP CAHN, J. DURHAM, P. HEATH, P. WRAY, R. PAVITT, J. WILKINSON, M. LEVERSHA, E. HUCKLE, CJ SHAW SMITH, A. DUNHAM, S. RHODES, V. SCHUSTER, G. PORTA, L. YIN, P. SERAFINI, B. SYLLA, ZOLLO, MASSIMO, A. BOLINO, M. SERI, A. LANYI, JR DAVIS, D. WEBSTER, A. HARRIS, G. LENOIR, G. DE ST BASILE, A. JONES, BH BEHLORADSKY, H. ACHATZ, J. MURKEN, R. FAESSLER, J. SUMEGI, G. ROMEO, M. VAUDIN, MT ROSS, A. MEINDL DR B.E.N.T.L.E.Y., FRANCO, BRUNELLA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::3200c944d05b0a0bc8fa6a9f3eb1f43a
http://hdl.handle.net/11588/143903
http://hdl.handle.net/11588/143903
Autor:
A. J. Mungall, S. A. Palmer, S. K. Sims, C. A. Edwards, J. L. Ashurst, L. Wilming, M. C. Jones, R. Horton, S. E. Hunt, C. E. Scott, J. G. R. Gilbert, M. E. Clamp, G. Bethel, S. Milne, R. Ainscough, J. P. Almeida, K. D. Ambrose, T. D. Andrews, R. I. S. Ashwell, A. K. Babbage, C. L. Bagguley, J. Bailey, R. Banerjee, D. J. Barker, K. F. Barlow, K. Bates, D. M. Beare, H. Beasley, O. Beasley, C. P. Bird, S. Blakey, S. Bray-Allen, J. Brook, A. J. Brown, J. Y. Brown, D. C. Burford, W. Burrill, J. Burton, C. Carder, N. P. Carter, J. C. Chapman, S. Y. Clark, G. Clark, C. M. Clee, S. Clegg, V. Cobley, R. E. Collier, J. E. Collins, L. K. Colman, N. R. Corby, G. J. Coville, K. M. Culley, P. Dhami, J. Davies, M. Dunn, M. E. Earthrowl, A. E. Ellington, K. A. Evans, L. Faulkner, M. D. Francis, A. Frankish, J. Frankland, L. French, P. Garner, J. Garnett, M. J. R. Ghori, L. M. Gilby, C. J. Gillson, R. J. Glithero, D. V. Grafham, M. Grant, S. Gribble, C. Griffiths, M. Griffiths, R. Hall, K. S. Halls, S. Hammond, J. L. Harley, E. A. Hart, P. D. Heath, R. Heathcott, S. J. Holmes, P. J. Howden, K. L. Howe, G. R. Howell, E. Huckle, S. J. Humphray, M. D. Humphries, A. R. Hunt, C. M. Johnson, A. A. Joy, M. Kay, S. J. Keenan, A. M. Kimberley, A. King, G. K. Laird, C. Langford, S. Lawlor, D. A. Leongamornlert, M. Leversha, C. R. Lloyd, D. M. Lloyd, J. E. Loveland, J. Lovell, S. Martin, M. Mashreghi-Mohammadi, G. L. Maslen, L. Matthews, O. T. McCann, S. J. McLaren, K. McLay, A. McMurray, M. J. F. Moore, J. C. Mullikin, D. Niblett, T. Nickerson, K. L. Novik, K. Oliver, E. K. Overton-Larty, A. Parker, R. Patel, A. V. Pearce, A. I. Peck, B. Phillimore, S. Phillips, R. W. Plumb, K. M. Porter, Y. Ramsey, S. A. Ranby, C. M. Rice, M. T. Ross, S. M. Searle, H. K. Sehra, E. Sheridan, C. D. Skuce, S. Smith, M. Smith, L. Spraggon, S. L. Squares, C. A. Steward, N. Sycamore, G. Tamlyn-Hall, J. Tester, A. J. Theaker, D. W. Thomas, A. Thorpe, A. Tracey, A. Tromans, B. Tubby, M. Wall, J. M. Wallis, A. P. West, S. S. White, S. L. Whitehead, H. Whittaker, A. Wild, D. J. Willey, T. E. Wilmer, J. M. Wood, P. W. Wray, J. C. Wyatt, L. Young, R. M. Younger, D. R. Bentley, A. Coulson, R. Durbin, T. Hubbard, J. E. Sulston, I. Dunham, J. Rogers, S. Beck
Publikováno v:
Nature. 425(6960)
Chromosome 6 is a metacentric chromosome that constitutes about 6% of the human genome. The finished sequence comprises 166,880,988 base pairs, representing the largest chromosome sequenced so far. The entire sequence has been subjected to high-quali
Publikováno v:
Biochimica et biophysica acta. 1490(1-2)
A putative novel murine serine protease, DISP, was identified by cDNA indexing and shown to be expressed primarily in distal gut. FISH analysis showed it to be localised to mouse chromosome 17A3. A possible human homologue for DISP has been identifie
Autor:
A M, Leversha, M I, Asher
Publikováno v:
The New Zealand medical journal. 109(1017)
Autor:
A M, Leversha, R E, Marks
Publikováno v:
The New Zealand medical journal. 108(1013)
To obtain an estimate of the prevalence of fetal alcohol syndrome in New Zealand and to report information on paediatrician surveillance for alcohol related birth defects.New Zealand paediatricians were asked to complete a postal survey. Questions re
Autor:
A M, Leversha, R E, Marks
Publikováno v:
The New Zealand medical journal. 108(1010)
This study was undertaken to gain an understanding about doctors' perspectives on alcohol consumption in pregnancy. The specific aim was to examine attitudes, knowledge and clinical practice of a sample of New Zealand doctors.A questionnaire was sent
In a tertiary referral centre 63 patients underwent 67 treatment periods with enalapril. The median age was 5.4 months. All children had signs of heart failure: congestive cardiac failure with breathlessness at rest was present in 88%. Haemodynamic g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba9aa65bbee532d2d4a41b667c1f69f5
https://europepmc.org/articles/PMC1029679/
https://europepmc.org/articles/PMC1029679/
Publikováno v:
Pediatric Research. 41:202-202
Objective: To examine the validity of an alternative Asian and Pacific Islander racial classification by comparing pregnancy outcomes among Asian and Pacific Islander (PI) subgroups.