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Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.
Genetics. 2014 Jul;197(3):1039-44. doi: 10.1534/genetics.114.165225. Epub 2014 May 2.
Genetics. 2014.
PMID: 24793288
Free PMC article.
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.
Bureau A, Younkin SG, Parker MM, Bailey-Wilson JE, Marazita ML, Murray JC, Mangold E, Albacha-Hejazi H, Beaty TH, Ruczinski I.
Bureau A, et al.
Bioinformatics. 2014 Aug 1;30(15):2189-96. doi: 10.1093/bioinformatics/btu198. Epub 2014 Apr 16.
Bioinformatics. 2014.
PMID: 24740360
Free PMC article.
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