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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 2 |
2012 | 3 |
2013 | 2 |
2024 | 0 |
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5 results
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Page 1
Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data.
Hum Mutat. 2013 Jul;34(7):945-52. doi: 10.1002/humu.22322. Epub 2013 Apr 29.
Hum Mutat. 2013.
PMID: 23554237
Autozygosity mapping with exome sequence data.
Carr IM, Bhaskar S, O'Sullivan J, Aldahmesh MA, Shamseldin HE, Markham AF, Bonthron DT, Black G, Alkuraya FS.
Carr IM, et al.
Hum Mutat. 2013 Jan;34(1):50-6. doi: 10.1002/humu.22220. Epub 2012 Oct 22.
Hum Mutat. 2013.
PMID: 23090942
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Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype.
Carr IM, Diggle CP, Khan K, Inglehearn C, McKibbin M, Bonthron DT, Markham AF, Anwar R, Dobbie A, Pena SD, Ali M.
Carr IM, et al.
PLoS One. 2012;7(8):e43466. doi: 10.1371/journal.pone.0043466. Epub 2012 Aug 17.
PLoS One. 2012.
PMID: 22912880
Free PMC article.
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Identification of autosomal recessive disease loci using out-bred nuclear families.
Carr IM, Diggle CP, Touqan N, Anwar R, Sheridan EG, Bonthron DT, Johnson CA, Ali M, Markham AF.
Carr IM, et al.
Hum Mutat. 2012 Feb;33(2):338-42. doi: 10.1002/humu.21645. Epub 2011 Nov 28.
Hum Mutat. 2012.
PMID: 22052625
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Estimating the degree of identity by descent in consanguineous couples.
Carr IM, Markham SA, Pena SD.
Carr IM, et al.
Hum Mutat. 2011 Dec;32(12):1350-8. doi: 10.1002/humu.21584. Epub 2011 Sep 23.
Hum Mutat. 2011.
PMID: 21901788
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