Author/Creator: Aldred, M A - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Aldred, M A

1. Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred. Issue 7 (July 1991)

Authors:: 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
Journal:: Journal of medical genetics
Issue:: Volume 28:Issue 7(1991)
Page Start:: 453
Record Type:: Journal Article
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2. Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorder. Issue 12 (2nd December 2005)

Authors:: Kinning, E; Tufarelli, C; Winship, W S; Aldred, M A; Trembath, R C
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 12(2005)
Page Start:: e70
Record Type:: Journal Article
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3. Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes. Issue 6 (1st June 2004)

Authors:: 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
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 6(2004)
Page Start:: 433
Record Type:: Journal Article
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4. Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci. Issue 11 (November 1994)

Authors:: Aldred, M A; Teague, P W; Jay, M; Bundey, S; Redmond, R M; Jay, B; Bird, A C; Bhattacharya, S S; Wright, A F
Journal:: Journal of medical genetics
Issue:: Volume 31:Issue 11(1994)
Page Start:: 848
Record Type:: Journal Article
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