Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes
Aldred, M A, Sanford, R O C, Thomas, N S, Barrow, M A, Wilson, L C, Brueton, L A, Bonaglia, M C, Hennekam, R C M, Eng, C, Dennis, N R, Trembath, R C
Published in Journal of medical genetics (01.06.2004)
Published in Journal of medical genetics (01.06.2004)
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Journal Article
Alveolar Epithelial Cells Up-Regulate microRNA-17 & microRNA-548b in Response to Cold Ischemia - Ex Vivo Reperfusion of Human Lungs
Elgharably, H., Okamoto, T., Ayyat, K.S., Niikawa, H., Meade, S., Farver, C., Chan, E., Aldred, M.A., McCurry, K.R.
Published in The Journal of heart and lung transplantation (01.04.2020)
Published in The Journal of heart and lung transplantation (01.04.2020)
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Journal Article
Three decades of occupational individual monitoring at the University of São Paulo
Okuno, E, Umisedo, N K, Cancio, F S, Aldred, M A, Yoshimura, E M
Published in Radiation protection dosimetry (01.12.2017)
Published in Radiation protection dosimetry (01.12.2017)
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Journal Article
Heterogeneity analysis in 40 X-linked retinitis pigmentosa families
TEAGUE, P. W, ALDRED, M. A, BUNDEY, S, JAY, B, BIRD, A. C, BHATTACHARYA, S. S, WRIGHT, A. F, JAY, M, DEMPSTER, M, HARRISON, C, CAROTHERS, A. D, HARDWICK, L. J, EVANS, H. J, STRAIN, L, BROCK, D. J. H
Published in American journal of human genetics (01.07.1994)
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Published in American journal of human genetics (01.07.1994)
Journal Article
Interstitial deletion constitutes the major mechanism for loss of heterozygosity on chromosome 20q in polycythemia vera
ASIMAKOPOULOS, F. A, GILBERT, J. G. R, ALDRED, M. A, PEARSON, T. C, GREEN, A. R
Published in Blood (01.10.1996)
Published in Blood (01.10.1996)
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Journal Article
How safe is ERCP to the endoscopist ?
COHEN, R. V, ALDRED, M. A, PAES, W. S, FAUSTO, A. M. F, NUCCI, J. R, YOSHIMURA, E. M, OKUNO, E, GARCIA, M. E, MARUTA, L. M, TOLOSA, E. M. C
Published in Surgical endoscopy (01.06.1997)
Published in Surgical endoscopy (01.06.1997)
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Journal Article
A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region
Bench, Anthony J., Aldred, Micheala A., Humphray, Sean J., Champion, Kim M., Gilbert, James G.R., Asimakopoulos, Fotios A., Deloukas, Panos, Gwilliam, Rhian, Bentley, David R., Green, Anthony R.
Published in Genomics (San Diego, Calif.) (01.05.1998)
Published in Genomics (San Diego, Calif.) (01.05.1998)
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Journal Article
Analysis of Three Deletion Breakpoints in Xp21.1 and the Further Localization of RP3
Brown, John, Dry, Katherine L., Edgar, Alexander J., Pryde, Fiona E., Hardwick, Lee J., Aldred, Micheala A., Lester, Douglas H., Boyle, Shelagh, Kaplan, Josseline, Dufier, Jean-Louis, Ho, Meng-Fatt, Monaco, Anthony M., Musarella, Maria A., Wright, Alan F.
Published in Genomics (San Diego, Calif.) (15.10.1996)
Published in Genomics (San Diego, Calif.) (15.10.1996)
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Journal Article
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred
Wright, A F, Bhattacharya, S S, Aldred, M A, Jay, M, Carothers, A D, Thomas, N S, Bird, A C, Jay, B, Evans, H J
Published in Journal of medical genetics (01.07.1991)
Published in Journal of medical genetics (01.07.1991)
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Journal Article
Linkage analysis in X-linked congenital stationary night blindness
Aldred, M.A., Dry, K.L., Sharp, D.M., Van Dorp, D.B., Brown, J., Hardwick, L.J., Lester, D.H., Pryde, F.E., Teague, P.W., Jay, M., Bird, A.C., Jay, B., Wright, A.F.
Published in Genomics (San Diego, Calif.) (01.09.1992)
Published in Genomics (San Diego, Calif.) (01.09.1992)
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Journal Article
Linkage analysis in a family with complete type congenital stationary night blindness with and without myopia
Dry, K L, Van Dorp, D B, Aldred, M A, Brown, J, Hardwick, L J, Wright, A F
Published in Clinical genetics (01.05.1993)
Published in Clinical genetics (01.05.1993)
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Journal Article
Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa
Aldred, M A, Dry, K L, Knight-Jones, E B, Hardwick, L J, Teague, P W, Lester, D H, Brown, J, Spowart, G, Carothers, A D, Raeburn, J A
Published in American journal of human genetics (01.11.1994)
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Published in American journal of human genetics (01.11.1994)
Journal Article
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci
Aldred, M A, Teague, P W, Jay, M, Bundey, S, Redmond, R M, Jay, B, Bird, A C, Bhattacharya, S S, Wright, A F
Published in Journal of medical genetics (01.11.1994)
Published in Journal of medical genetics (01.11.1994)
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