Author/Creator: White, S J - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator White, S J

1. An alternative to FISH: detecting deletion and duplication carriers within 24 hours. Issue 10 (20th October 2003)

Authors:: White, S J; Sterrenburg, E; van Ommen, G-J B; den Dunnen, J T; Breuning, M H
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 10(2003)
Page Start:: e113
Record Type:: Journal Article
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2. Contribution of Fcγ receptor IIIA gene 158V/F polymorphism and copy number variation to the risk of ACPA-positive rheumatoid arthritis. Issue 11 (19th November 2008)

Authors:: Thabet, M M; Huizinga, T W J; Marques, R B; Stoeken-Rijsbergen, G; Bakker, A M; Kurreeman, F A; White, S J; Toes, R E M; van der Helm-van Mil, A H M
Journal:: Annals of the rheumatic diseases
Issue:: Volume 68:Issue 11(2009)
Page Start:: 1775
Record Type:: Journal Article
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3. Exploring elderly patients' perspectives on deprescribing: a qualitative study interim analysis. (1st April 2022)

Authors:: Channa, K K; Venables, R H; White, S J
Journal:: International journal of pharmacy practice
Issue:: Volume 30(2022)Supplement 1
Page Start:: i1
Record Type:: Journal Article
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4. Genomic imbalances in mental retardation. Issue 4 (1st April 2004)

Authors:: Kriek, M; White, S J; Bouma, M C; Dauwerse, H G; Hansson, K B M; Nijhuis, J V; Bakker, B; van Ommen, G-J B; den Dunnen, J T; Breuning, M H
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 4(2004)
Page Start:: 249
Record Type:: Journal Article
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5. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification. Issue 12 (13th May 2005)

Authors:: Harteveld, C L; Voskamp, A; Phylipsen, M; Akkermans, N; den Dunnen, J T; White, S J; Giordano, P C
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 12(2005)
Page Start:: 922
Record Type:: Journal Article
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6. Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers. Issue 7 (July 1991)

Authors:: Mulley, J C; Gedeon, A K; White, S J; Haan, E A; Richards, R I
Journal:: Journal of medical genetics
Issue:: Volume 28:Issue 7(1991)
Page Start:: 448
Record Type:: Journal Article
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7. Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctata. Issue 12 (December 1998)

Authors:: Sheffield, L J; Osborn, A H; Hutchison, W M; Sillence, D O; Forrest, S M; White, S J; Dahl, H H
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 12(1998)
Page Start:: 1004
Record Type:: Journal Article
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