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Allele sharing at 12/15 STR loci between full siblings.
Pontikinas E, Attwell M, Nicholls C. Pontikinas E, et al. Among authors: nicholls c. Forensic Sci Int Genet. 2015 May;16:163-164. doi: 10.1016/j.fsigen.2015.01.003. Epub 2015 Jan 16. Forensic Sci Int Genet. 2015. PMID: 25618748 No abstract available.
Three step maternal mutation detected by STR analysis.
Attwell M, Pontikinas E, Nicholls C. Attwell M, et al. Among authors: nicholls c. Forensic Sci Int Genet. 2015 May;16:138. doi: 10.1016/j.fsigen.2015.01.004. Epub 2015 Jan 9. Forensic Sci Int Genet. 2015. PMID: 25600396 No abstract available.
Novel protein C gene mutation in a compound heterozygote resulting in catastrophic thrombosis in early adulthood: diagnosis and long-term treatment with subcutaneous protein C concentrate.
Boey JP, Jolley A, Nicholls C, Lerda N, Duncan E, Gallus A, Ross DM, Sobieraj-Teague M. Boey JP, et al. Among authors: nicholls c. Br J Haematol. 2016 Mar;172(5):811-3. doi: 10.1111/bjh.13538. Epub 2015 Jun 24. Br J Haematol. 2016. PMID: 26103879 Free article. No abstract available.
Male carrier of haemophilia A.
Williams VK, Liebelt J, Nicholls C, Reardon S, Suppiah R. Williams VK, et al. Among authors: nicholls c. Pathology. 2014 Aug;46(5):467-8. doi: 10.1097/PAT.0000000000000131. Pathology. 2014. PMID: 24992242 No abstract available.
147 results