Points to consider for providing expert witness testimony for the specialty of medical genetics: A statement of the American College of Medical Genetics and Genomics (ACMG) von Seaver, Laurie H., Chan, Perry, Fleisher, Lynn D., Huang, Samuel J., Klugman, Susan D., Matalon, Dena R.

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Reporting genomic secondary findings: ACMG members weigh in von Scheuner, Maren T., Peredo, Jane, Benkendorf, Judith, Bowdish, Bruce, Feldman, Gerald, Fleisher, Lynn, Mulvihill, John J., Watson, Michael, Herman, Gail E., Evans, James

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Technical report: ethical and policy issues in genetic testing and screening of children von Ross, Laine Friedman, Saal, Howard M., David, Karen L., Anderson, Rebecca R.

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Appropriate use of the designation of ABO certification: A Statement by the American Board of Orthodontics von Moffitt, Allen H., Greco, Peter M., Fleisher, Lynn D.

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Update on HIPAA privacy: are you ready? von Cole, Laura J, Fleisher, Lynn D

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Newborn screening: toward a uniform screening panel and system--executive summary von Watson, Michael S., Mann, Marie Y., Lloyd-Puryear, Michele A., Rinaldo, Piero, Howell, R. Rodney

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Update on HIPAA privacy: Are you ready? von Cole, Laura J., Fleisher, Lynn D.

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Genetics in Medicine inaugurates legal section von Fleisher, Lynn D.

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Duty to re-contact von Hirschhorn, K, Fleisher, L D, Godmilow, L, Howell, R R, Lebel, R R, McCabe, E R, McGinniss, M J, Milunsky, A, Pelias, M Z, Pyeritz, R E, Sujansky, E, Thompson, B H, Zinberg, R E

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Health Insurance Portability and Accountability Act is here: What price privacy? von Fleisher, Lynn D., Cole, Laura J.

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Carnosinase deficiency: a new variant with high residual activity von Fleisher, L D, Rassin, D K, Wisniewski, K, Salwen, H R

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Cystathionine beta-synthase deficiency: differences in thermostability between normal and abnormal enzyme from cultured human cells von Fleisher, L D, Longhi, R C, Tallan, H H, Gaull, G E

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714 EXPERIENCE IN THE PRENATAL DIAGNOSIS OF ARGININO-SUCCINIC ACID (ASA) URIA AND CITRULLINEMIA von Fleisher, Lynn D, Salwen, Helen R, Nadler, Henry L

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Cystathionine synthase deficiency: Heterozygote detection using cultured skin fibroblasta von Fleisher, Lynn D., Tallan, Harris H., Beratis, Nicholas G., Hirschhorn, Kurt, Gaull, Gerald E.

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Cystathionine beta-synthase deficiency: a qualitative abnormality of the deficient enzyme modified by vitamin B6 therapy von Longhi, R C, Fleisher, L D, Tallan, H H, Gaull, G E

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3Methionine metabolism in man: Development and deficiencies von Fleisher, Lynn D., Gaull, Gerald E.

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Fetal tissue amino acid concentrations in argininosuccinic aciduria and in “maternal homocystinuria” von Rassin, David K., Fleisher, Lynn D., Muir, Angus, Desnick, Robert J., Gaull, Gerald E.

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DETECTION OF CYSTATHIONINE SYNTHASE IN LONG-TERM LYMPHOID-CELL LINES von Fleisher, LynnD, Beratis, NicholasG, Hirschhorn, Kurt, Gaull, GeraldE

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Brief of the American Medical Association, "et al". as "Amici Curiae" in Support of Appellees von Johnson, Kirk B, Hirshfeld, Edward B, Orentlicher, David, Lawton, Stephan E, Allen, Ann E, Bierig, Jack R, Graham, David F, Fleisher, Lynn D, Phillips, Carter G, Esty, Elizabeth H, Farris, Juli E

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Hawkinsinuria in two families von Borden, Margaret, Holm, Jan, Leslie, Jack, Sweetman, Lawrence, Nyhan, William L., Fleisher, Lynn, Nadler, Henry, Lewis, David, Scott, C. Ronald

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