Redman JB - Search Results

1

Improving accuracy of Tay Sachs carrier screening of the non-Jewish population: analysis of 34 carriers and six late-onset patients with HEXA enzyme and DNA sequence analysis.

Park NJ, Morgan C, Sharma R, Li Y, Lobo RM, Redman JB, Salazar D, Sun W, Neidich JA, Strom CM. Park NJ, et al. Among authors: redman jb. Pediatr Res. 2010 Feb;67(2):217-20. doi: 10.1203/PDR.0b013e3181c6e318. Pediatr Res. 2010. PMID: 19858779

2

Cystic fibrosis testing 8 years on: lessons learned from carrier screening and sequencing analysis.

Strom CM, Crossley B, Buller-Buerkle A, Jarvis M, Quan F, Peng M, Muralidharan K, Pratt V, Redman JB, Sun W. Strom CM, et al. Among authors: redman jb. Genet Med. 2011 Feb;13(2):166-72. doi: 10.1097/GIM.0b013e3181fa24c4. Genet Med. 2011. PMID: 21068670 Free article.

3

Frequency of the cystic fibrosis 3199del6 mutation in individuals heterozygous for I148T.

Buller A, Olson S, Redman JB, Hantash F, Chen R, Strom CM. Buller A, et al. Among authors: redman jb. Genet Med. 2004 Mar-Apr;6(2):108-9. doi: 10.1097/01.gim.0000117332.18002.ff. Genet Med. 2004. PMID: 15017334 Free article.

4

Cystic fibrosis screening: lessons learned from the first 320,000 patients.

Strom CM, Crossley B, Redman JB, Buller A, Quan F, Peng M, McGinnis M, Sun W. Strom CM, et al. Among authors: redman jb. Genet Med. 2004 May-Jun;6(3):136-40. doi: 10.1097/01.gim.0000127268.65149.69. Genet Med. 2004. PMID: 15354331

5

Molecular screening for diseases frequent in Ashkenazi Jews: lessons learned from more than 100,000 tests performed in a commercial laboratory.

Strom CM, Crossley B, Redman JB, Quan F, Buller A, McGinniss MJ, Sun W. Strom CM, et al. Among authors: redman jb. Genet Med. 2004 May-Jun;6(3):145-52. doi: 10.1097/01.gim.0000127267.57526.d1. Genet Med. 2004. PMID: 15354333

6

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. Among authors: redman jb. Genet Med. 2005 Apr;7(4):278-82. doi: 10.1097/01.gim.0000159904.92850.d5. Genet Med. 2005. PMID: 15834246 Free article.

7

Extensive sequencing of the CFTR gene: lessons learned from the first 157 patient samples.

McGinniss MJ, Chen C, Redman JB, Buller A, Quan F, Peng M, Giusti R, Hantash FM, Huang D, Sun W, Strom CM. McGinniss MJ, et al. Among authors: redman jb. Hum Genet. 2005 Dec;118(3-4):331-8. doi: 10.1007/s00439-005-0065-1. Epub 2005 Sep 28. Hum Genet. 2005. PMID: 16189704

8

Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening.

Hantash FM, Redman JB, Starn K, Anderson B, Buller A, McGinniss MJ, Quan F, Peng M, Sun W, Strom CM. Hantash FM, et al. Among authors: redman jb. Hum Genet. 2006 Mar;119(1-2):126-36. doi: 10.1007/s00439-005-0082-0. Epub 2005 Dec 17. Hum Genet. 2006. PMID: 16362824

9

Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator gene.

Hantash FM, Redman JB, Goos D, Kammesheidt A, McGinniss MJ, Sun W, Strom CM. Hantash FM, et al. Among authors: redman jb. J Mol Diagn. 2007 Sep;9(4):556-60. doi: 10.2353/jmoldx.2007.060141. Epub 2007 Aug 9. J Mol Diagn. 2007. PMID: 17690208 Free PMC article.

10

Apparent homozygosity of a novel frame shift mutation in the CFTR gene because of a large deletion.

Hantash FM, Rebuyon A, Peng M, Redman JB, Sun W, Strom CM. Hantash FM, et al. Among authors: redman jb. J Mol Diagn. 2009 May;11(3):253-6. doi: 10.2353/jmoldx.2009.080117. Epub 2009 Mar 26. J Mol Diagn. 2009. PMID: 19324987 Free PMC article.

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