Pike-Buchanan LL - Search Results

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Genotype-phenotype correlation and frequency of the 3199del6 cystic fibrosis mutation among I148T carriers: results from a collaborative study.

Monaghan KG, Highsmith WE, Amos J, Pratt VM, Roa B, Friez M, Pike-Buchanan LL, Buyse IM, Redman JB, Strom CM, Young AL, Sun W. Monaghan KG, et al. Among authors: pike buchanan ll. Genet Med. 2004 Sep-Oct;6(5):421-5. doi: 10.1097/01.GIM.0000139507.20179.3A. Genet Med. 2004. PMID: 15371907 Free article.

Detection of 677CT/1298AC "double variant" chromosomes: implications for interpretation of MTHFR genotyping results.

Brown NM, Pratt VM, Buller A, Pike-Buchanan L, Redman JB, Sun W, Chen R, Crossley B, McGinniss MJ, Quan F, Strom CM. Brown NM, et al. Genet Med. 2005 Apr;7(4):278-82. doi: 10.1097/01.gim.0000159904.92850.d5. Genet Med. 2005. PMID: 15834246 Free article.

Identification of cystic fibrosis variants by polymerase chain reaction/oligonucleotide ligation assay.

Schwartz KM, Pike-Buchanan LL, Muralidharan K, Redman JB, Wilson JA, Jarvis M, Cura MG, Pratt VM. Schwartz KM, et al. Among authors: pike buchanan ll. J Mol Diagn. 2009 May;11(3):211-5. doi: 10.2353/jmoldx.2009.080106. Epub 2009 Mar 26. J Mol Diagn. 2009. PMID: 19324992 Free PMC article.

Molecular testing: improving patient care through partnering with laboratory genetic counselors.

Scacheri C, Redman JB, Pike-Buchanan L, Steenblock K. Scacheri C, et al. Genet Med. 2008 May;10(5):337-42. doi: 10.1097/GIM.0b013e31817283a5. Genet Med. 2008. PMID: 18496032 Free article.

Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA.

Reddy PH, Williams M, Charles V, Garrett L, Pike-Buchanan L, Whetsell WO Jr, Miller G, Tagle DA. Reddy PH, et al. Nat Genet. 1998 Oct;20(2):198-202. doi: 10.1038/2510. Nat Genet. 1998. PMID: 9771716

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