Redman JB - Search Results

1

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: redman jb. Genet Med. 2004 Sep-Oct;6(5):421-5. doi: 10.1097/01.GIM.0000139507.20179.3A. Genet Med. 2004. PMID: 15371907 Free article.

2

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.

3

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

4

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.

5

The dangers of including nonclassical cystic fibrosis variants in population-based screening panels: p.L997F, further genotype/phenotype correlation data.

Strom CM, Redman JB, Peng M. Strom CM, et al. Among authors: redman jb. Genet Med. 2011 Dec;13(12):1042-4. doi: 10.1097/GIM.0b013e318228efb2. Genet Med. 2011. PMID: 21804385 Free article.

6

Cystic fibrosis screening using the College panel: platform comparison and lessons learned from the first 20,000 samples.

Strom CM, Huang D, Buller A, Redman J, Crossley B, Anderson B, Entwistle T, Sun W. Strom CM, et al. Genet Med. 2002 Jul-Aug;4(4):289-96. doi: 10.1097/00125817-200207000-00007. Genet Med. 2002. PMID: 12172395 Free article.

7

Extensive sequencing of the cystic fibrosis transmembrane regulator gene: assay validation and unexpected benefits of developing a comprehensive test.

Strom CM, Huang D, Chen C, Buller A, Peng M, Quan F, Redman J, Sun W. Strom CM, et al. Genet Med. 2003 Jan-Feb;5(1):9-14. doi: 10.1097/00125817-200301000-00002. Genet Med. 2003. PMID: 12544470 Free article.

8

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

9

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

10

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

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