Michele Ramsay to Mutation
This is a "connection" page, showing publications Michele Ramsay has written about Mutation.
Connection Strength
0,891
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MYOC mutations in black south african patients with primary open-angle glaucoma: genetic testing and cascade screening. Ophthalmic Genet. 2015 Mar; 36(1):31-8.
Score: 0,425
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CFTR structural rearrangements are not a major mutational mechanism in black and coloured southern African patients with cystic fibrosis. S Afr Med J. 2009 Oct; 99(10):724.
Score: 0,300
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Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population. Int J Pediatr Otorhinolaryngol. 2011 May; 75(5):611-7.
Score: 0,083
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Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1). Hum Mol Genet. 2002 Apr 01; 11(7):833-40.
Score: 0,045
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Myocilin mutations in black South Africans with POAG. Mol Vis. 2011 Apr 27; 17:1064-9.
Score: 0,021
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WGA allows the molecular characterization of a novel large CFTR rearrangement in a black South African cystic fibrosis patient. J Mol Diagn. 2008 Nov; 10(6):544-8.
Score: 0,017