US Newborn Screening System Guidelines II: Follow-up of Children, Diagnosis, Management, and Evaluation Statement of the Council of Regional Networks for Genetic Services (CORN) von Pass, Kenneth A., Lane, Peter A., Fernhoff, Paul M., Hinton, Cynthia F., Panny, Susan R., Parks, John S., Pelias, Mary Z., Rhead, William J., Ross, Sonya I., Wethers, Doris L., Elsas, Louis J.

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Federal regulations and the future of research in human and medical genetics von Pelias, Mary Z.

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The USH1C 216G-->A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population von Savas, Sevtap, Frischhertz, Ben, Pelias, Mary Z, Batzer, Mark A, Deininger, Prescott L, Keats, Bronya B

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Assembly of a high-resolution map of the Acadian Usher syndrome region and localization of the nuclear EF-hand acidic gene von DeAngelis, Margaret M., Doucet, John P., Drury, Stacy, Sherry, Stephen T., Robichaux, Myles B., Den, Zhining, Pelias, Mary Z., Ditta, Gregory M., Keats, Bronya J.B., Deininger, Prescott L., Batzer, Mark A.

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Decreased content of docosahexaenoate and arachidonate in plasma phospholipids in usher's syndrome von Bazan, Nicolas G., Scott, Burton L., Reddy, T.S., Pelias, Mary Z.

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Localization of two genes for usher syndrome type I to chromosome 11 von Smith, Richard J.H., Lee, Elizabeth C., Kimberling, William J., Daiger, Stephen P., Pelias, Mary Z., Keats, Bronya J.B., Jay, Marcelle, Bird, Alan, Reardon, William, Guest, Mary, Ayyagari, Radha, Fielding Hejtmancik, J.

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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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Recent Developments in Human Behavioral Genetics: Past Accomplishments and Future Directions von Sherman, Stephanie L., DeFries, John C., Gottesman, Irving I., Loehlin, John C., Meyer, Joanne M., Pelias, Mary Z., Rice, John, Waldman, Irwin

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Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11 von Keats, B J, Nouri, N, Pelias, M Z, Deininger, P L, Litt, M

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Response to Allegations against James V. Neel in Darkness in El Dorado, by Patrick Tierney

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The USHIC 216G→A mutation and the 9-repeat VNTR(t, t) allele are in complete linkage disequilibrium in the Acadian population von SAVAS, Sevtap, FRISCHHERTZ, Ben, PELIAS, Mary Z, BATZER, Mark A, DEININGER, Prescott L, KEATS, Bronya J. B

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The Human Genome Project and public perception: truth and consequences von Pelias, M Z, Markward, N J

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A sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome von Pelias, Mary Z., Superneau, Duane W., Thurmon, Theodore F., Opitz, John M.

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Linkage studies of usher syndrome type 1: Exclusion results from the usher syndrome consortium von Keats, Bronya J.B., Todorov, Alexander A., Atwood, Larry D., Pelias, Mary Z., Hejtmancik, J. Fielding, Kimberling, William J., Leppert, Mark, Lewis, Richard A., Smith, Richard J.H.

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Clinical variability and genetic heterogeneity within the Acadian Usher population von Smith, Richard J. H., Pelias, Mary Z., Daiger, Stephen P., Keats, Bronya, Kimberling, William, Hejtmancik, J. Fielding

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Duty to disclose: Response to Dr. Borgaonkar von Pelias, Mary Z.

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Duty to disclose in medical genetics: A legal perspective von Pelias, Mary Z.

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The duty to disclose to relatives in medical genetics: Response to Dr. Hecht von Pelias, Mary Z.

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Genetic studies in multiple myeloma 1. Association with HLA‐Cw5 von Leech, Stephen H., Bryan, Christopher F., Elston, Robert C., Rainey, John, Bickers, John N., Pelias, Mary Z.

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Torts of wrongful birth and wrongful life: A review von Pelias, Mary Z., Shaw, Margery W.

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