Genotype-phenotype correlation and frequency of the 3199del6 cystic fibrosis mutation among I148T carriers: Results from a collaborative study von Monaghan, K.G., Highsmith, W.E., Amos, J., Pratt, V.M., Roa, B., Friez, M., Pike-Buchanan, L.L., Buyse, I.M., Redman, J.B., Strom, C.M., Young, A.L., Sun, W.

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Novel and recurrent rearrangements in the CFTR gene : clinical and laboratory implications for cystic fibrosis screening von HANTASH, Feras M, REDMAN, Joy B, STARN, Kelsey, ANDERSON, Ben, BULLER, Arlene, MCGINNISS, Matthew J, QUAN, Franklin, MEI PENG, WEIMIN SUN, STROM, Charles M

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Cystic fibrosis screening: Lessons learned from the first 320,000 patients von Strom, Charles M., Crossley, Beryl, Redman, Joy B., Buller, Arlene, Quan, Franklin, Peng, Mei, McGinnis, Matthew, Sun, Weimin

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Molecular screening for diseases frequent in Ashkenazi Jews: Lessons learned from more than 100,000 tests performed in a commercial laboratory von Strom, Charles M., Crossley, Beryl, Redman, Joy B., Quan, Franklin, Buller, Arlene, McGinniss, Matthew J., Sun, Weimin

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Detection of 677CT/1298AC “double variant” chromosomes: Implications for interpretation of MTHFR genotyping results von Brown, Nicholas M., Pratt, Victoria M., Buller, Arlene, Pike-Buchanan, Lisa, Redman, Joy B., Sun, Weimin, Chen, Rebecca, Crossley, Beryl, McGinniss, Matthew J., Quan, Franklin, Strom, Charles M.

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Cystic fibrosis testing 8 years on: Lessons learned from carrier screening and sequencing analysis von Strom, Charles M., Crossley, Beryl, Buller-Buerkle, Arlene, Jarvis, Michael, Quan, Franklin, Peng, Mei, Muralidharan, Kasinathan, Pratt, Victoria, Redman, Joy B., Sun, Weimin

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Frequency of the cystic fibrosis 3199del6 mutation in individuals heterozygous for I148T von Buller, Arlene, Olson, Susan, Redman, Joy B., Hantash, Feras, Chen, Rebecca, Strom, Charles M.

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The dangers of including nonclassical cystic fibrosis variants in population-based screening panels: p.L997F, further genotype/phenotype correlation data von Strom, Charles M, Redman, Joy B, Peng, Mei

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Lesch-Nyhan syndrome: Carrier and prenatal diagnosis von Alford, R. L., Redman, J. B., O'brien, W. E., Caskey, C. T.

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Molecular testing for Fragile X Syndrome: lessons learned from 119,232 tests performed in a clinical laboratory von Strom, Charles M, Crossley, Beryl, Redman, Joy B, Buller, Arlene, Quan, Franklin, Peng, Mei, McGinnis, Matthew, Fenwick, Jr, Raymond G, Sun, Weimin

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Molecular testing: improving patient care through partnering with laboratory genetic counselors von Scacheri, Cheryl, Redman, Joy B., Pike-Buchanan, Lisa, Steenblock, Kelle

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Extensive sequencing of the CFTR gene : lessons learned from the first 157 patient samples von MCGINNISS, Matthew J, CHEN, Christina, STROM, Charles M, REDMAN, Joy B, BULLER, Arlene, QUAN, Franklin, MEI PENG, GIUSTI, Robert, HANTASH, Feras M, DONGHUI HUANG, WEIMIN SUN

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Validation and Clinical Application of a Locus-Specific Polymerase Chain Reaction- and Minisequencing-Based Assay for Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) von Keen-Kim, Dianne, Redman, Joy B., Alanes, Reno U., Eachus, Michele M., Wilson, Robert C., New, Maria I., Nakamoto, Jon M., Fenwick, Raymond G.

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Sabbatarian Accommodation in the Supreme Court von REDMAN, BARBARA J.

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Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening von Hantash, Feras M., Redman, Joy B., Starn, Kelsey, Anderson, Ben, Buller, Arlene, McGinniss, Matthew J., Quan, Franklin, Peng, Mei, Sun, Weimin, Strom, Charles M.

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River Thames-Abnormal High Tides von REDMAN, J. B

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River Thames-Abnormal High Tides von REDMAN, J. B

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Sea-Shore Alluvion, Dungeness von REDMAN, J. B

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River Thames-Abnormal High Tides von REDMAN, J. B

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Sea-shore Alluvion-the "Chesil" von REDMAN, J. B

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