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Year Number of Results
1990 1
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2011 1
2013 1
2014 1
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2019 2
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15 results

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Page 1
Expanding the phenotypic spectrum of Chromosome 16p13.11 microduplication: A multicentric analysis of 206 patients.
Hamad A, Sherlaw-Sturrock CA, Glover K, Salmon R, Low K, Nair R, Sansbury FH, Rawlins L, Carmichael J, Horton R, Wedderburn S, Edgerley K, Irving R, Callaghan M, Mercer C, McGowan R, Robert L, Titheradge H, Naik S. Hamad A, et al. Among authors: wedderburn s. Eur J Med Genet. 2023 Apr;66(4):104714. doi: 10.1016/j.ejmg.2023.104714. Epub 2023 Jan 29. Eur J Med Genet. 2023. PMID: 36724812
Skin lesions. The GP's view.
Wedderburn S. Wedderburn S. Br J Hosp Med. 1993 Feb 3-16;49(3):151-3. Br J Hosp Med. 1993. PMID: 8439782 No abstract available.
Towards establishing consistency in triage in a tertiary specialty.
McVeigh TP, Donnelly D, Al Shehhi M, Jones EA, Murray A, Wedderburn S, Porteous M, Lynch SA. McVeigh TP, et al. Among authors: wedderburn s. Eur J Hum Genet. 2019 Apr;27(4):547-555. doi: 10.1038/s41431-018-0322-0. Epub 2019 Jan 8. Eur J Hum Genet. 2019. PMID: 30622329 Free PMC article.
Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing.
Hocking LJ, Andrews C, Armstrong C, Ansari M, Baty D, Berg J, Bradley T, Clark C, Diamond A, Doherty J, Lampe A, McGowan R, Moore DJ, O'Sullivan D, Purvis A, Santoyo-Lopez J, Westwood P, Abbott M, Williams N; Scottish Genomes Partnership; Aitman TJ, Miedzybrodzka Z. Hocking LJ, et al. Eur J Hum Genet. 2023 Feb;31(2):231-238. doi: 10.1038/s41431-022-01226-3. Epub 2022 Dec 6. Eur J Hum Genet. 2023. PMID: 36474026 Free PMC article.
Grampian Health Board's joint drug formulary.
Garvey G, Jappy B, Stewart D, Williams A, Duffus PR, Maitland JM, Valentine MJ, Wedderburn S, Webster J, Petrie JC. Garvey G, et al. Among authors: wedderburn s. BMJ. 1990 Oct 13;301(6756):851-2. doi: 10.1136/bmj.301.6756.851. BMJ. 1990. PMID: 2282424 Free PMC article.
15 results