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Incorrect use of the term synteny.
Passarge E, Horsthemke B, Farber RA. Passarge E, et al. Among authors: farber ra. Nat Genet. 1999 Dec;23(4):387. doi: 10.1038/70486. Nat Genet. 1999. PMID: 10581019 No abstract available.
Screening for truncated NF1 proteins.
Heim RA, Silverman LM, Farber RA, Kam-Morgan LN, Luce MC. Heim RA, et al. Among authors: farber ra. Nat Genet. 1994 Nov;8(3):218-9. doi: 10.1038/ng1194-218. Nat Genet. 1994. PMID: 7874161 No abstract available.
Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction.
Fan H, Civalier C, Booker JK, Gulley ML, Prior TW, Farber RA. Fan H, et al. Among authors: farber ra. J Mol Diagn. 2006 May;8(2):277-81. doi: 10.2353/jmoldx.2006.050066. J Mol Diagn. 2006. PMID: 16645216 Free PMC article.
Mosaicism for an FMR1 gene deletion in a fragile X female.
Fan H, Booker JK, McCandless SE, Shashi V, Fleming A, Farber RA. Fan H, et al. Among authors: farber ra. Am J Med Genet A. 2005 Jul 15;136(2):214-7. doi: 10.1002/ajmg.a.30807. Am J Med Genet A. 2005. PMID: 15940701
52 results