Author/Creator: Williams, H - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Williams, H

61. The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. Issue 12 (December 1998)

Authors:: Kehoe, P G; Williams, H; Holmans, P; Wilcock, G; Cairns, N J; Neal, J; Owen, M J
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 12(1998)
Page Start:: 1034
Record Type:: Journal Article
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62. The use of flanking markers in prediction for Duchenne muscular dystrophy. Issue 3 (March 1986)

Authors:: Williams, H; Sarfarazi, M; Brown, C; Thomas, N; Harper, P S
Journal:: Archives of disease in childhood
Issue:: Volume 61:Issue 3(1986)
Page Start:: 218
Record Type:: Journal Article
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63. Toxoplasmosis. Issue 6264 (21st February 1981)

Authors:: Williams, H
Journal:: BMJ
Issue:: Volume 282:Issue 6264(1981)
Page Start:: 653
Record Type:: Journal Article
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64. Twice daily versus four times daily treatment with beclomethasone dipropionate in the control of mild childhood asthma. Issue 8 (August 1986)

Authors:: Williams, H; Jones, E R; Sibert, J R
Journal:: Thorax
Issue:: Volume 41:Issue 8(1986)
Page Start:: 602
Record Type:: Journal Article
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65. Widening participation in West Hertfordshire Hospices: enhancing access and diversity. (1st April 2011)

Authors:: Williams, H; Papadopoulos, I; Kelly, D
Journal:: BMJ supportive & palliative care
Issue:: Volume 1(2011)Supplement 1
Page Start:: A12
Record Type:: Journal Article
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66. X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci. Issue 5 (May 1990)

Authors:: Thomas, N S; Williams, H; Cole, G; Roberts, K; Clarke, A; Liechti-Gallati, S; Braga, S; Gerber, A; Meier, C; Moser, H
Journal:: Journal of medical genetics
Issue:: Volume 27:Issue 5(1990)
Page Start:: 284
Record Type:: Journal Article
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