Genetics and Phenotypes of RPE65 Mutations in Inherited Retinal Degeneration von Thompson, Debra A, Gyurus, Peter, Fleischer, Laura L, Bingham, Eve L, McHenry, Christina L, Apfelstedt-Sylla, Eckart, Zrenner, Eberhart, Lorenz, Birgit, Richards, Julia E, Jacobson, Samuel G, Sieving, Paul A, Gal, Andreas

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Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave von Sieving, Paul A, Bingham, Eve L, Kemp, Jennifer, Richards, Julia, Hiriyanna, K

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Dark-Light: Model for Nightblindness from the Human Rhodopsin Gly-90 → Asp Mutation von Sieving, Paul A., Richards, Julia E., Naarendorp, Franklin, Bingham, Eve L., Scott, Kathy, Alpern, Mathew

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The process of leaving an abusive relationship : The role of risk assessments and decision-certainty von MARTIN, A. J, BERENSON, K. R, GRIFFING, S, SAGE, R. E, MADRY, L, BINGHAM, L. E, PRIMM, B. J

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Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy von AYYAGARI, R, KAKUK, L. E, BINGHAM, E. L, SZCZESNY, J. J, KEMP, J, TODA, Y, FELIUS, J, SIEVING, P. A

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Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene von Ayyagari, R, Kakuk, L E, Coats, C L, Bingham, E L, Toda, Y, Felius, J, Sieving, P A

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Detection of Philadelphia Chromosome-Positive Cells by the Polymerase Chain Reaction Following Bone Marrow Transplant for Chronic Myelogenous Leukemia von Roth, M.S., Antin, J.H., Bingham, E.L., Ginsburg, D.

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Domestic Violence Survivors' Self-Identified Reasons for Returning to Abusive Relationships von Griffing, Sascha, Ragin, Deborah Fish, Sage, Robert E., Madry, Lorraine, Bingham, Lewis E., Primm, Beny J.

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Use of polymerase chain reaction-detected sequence polymorphisms to document engraftment following allogeneic bone marrow transplantation von ROTH, M. S, ANTIN, J. H, BINGHAM, E. L, GINSBURG, D

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Identification and Characterization of the Human Homologue (RAI2) of a Mouse Retinoic Acid-Induced Gene in Xp22 von Walpole, Susannah M., Hiriyana, Kelaginamane T., Nicolaou, Alexia, Bingham, Eve L., Durham, Jillian, Vaudin, Mark, Ross, Mark T., Yates, John R.W., Sieving, Paul A., Trump, Dorothy

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Phenotypic Expression of Juvenile X-linked Retinoschisis in Swedish Families With Different Mutations in the XLRS1 Gene von Eksandh, Louise C, Ponjavic, Vesna, Ayyagari, Radha, Bingham, Eve L, Hiriyanna, Kelaginamane T, Andréasson, Sten, Ehinger, Berndt, Sieving, Paul A

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Rearrangement of immunoglobulin and T-cell receptor genes in Hodgkin's disease von Roth, MS, Schnitzer, B, Bingham, EL, Harnden, CE, Hyder, DM, Ginsburg, D

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Refined Genetic Mapping of Juvenile X-Linked Retinoschisis von Pawar, Hemant, Bingham, Eve L., Lunetta, Kathryn L., Segal, Meridee, Richards, Julia E., Sieving, Paul A.

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Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change von Hiriyanna, Kelaginamane T., Bingham, Eve L., Yashar, Beverly M., Ayyagari, Radha, Fishman, Gerald, Small, Kent W., Weinberg, David V., Weleber, Richard G., Lewis, Richard A., Andreasson, Sten, Richards, Julia E., Sieving, Paul A.

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Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes von SIEVING, P. A, BINGHAM, E. L, ROTH, M. S, YOUNG, M. R, BOEHNKE, M, CHEN-YU KUO, GINSBURG, D

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X-Linked Juvenile Retinoschisis: Localization between (DXS1195, DXS418) and AFM291wf5 on a Single YAC von Pawar, Hemant, Bingham, Eve L., Hiriyanna, Kelaginamane, Segal, Meridee, Richards, Julia E., Sieving, Paul A.

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Linkage Study of Best's Vitelliform Macular Dystrophy (VMD2) in a Large North American Family von Hou, Yu-Chih, Richards, Julia E., Bingham, Eve L., Pawar, Hemant, Scott, Kathy, Segal, Meridee, Lunetta, Kathryn L., Boehnke, Michael, Sieving, Paul A.

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Intergenerational Substance Abuse and Domestic Violence as Familial Risk Factors for Lifetime Attempted Suicide Among Battered Women von Ragin, Deborah Fish, Pilotti, Mauta, Madry, Lorraine, Sage, Robert E, Bingham, Lewis E, Primm, Beny J

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A Colombian family with X-linked juvenile retinoschisis with three affected females: Finding of a frameshift mutation von Mendoza-Londono, R., Hiriyanna, K.T., Bingham, E.L., Rodriguez, F., Shastry, B.S., Rodriguez, A., Sieving, P.A., Tamayo, M.L.

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Bietti Crystalline Retinopathy and Juvenile Retinoschisis in a Family With a Novel RS1 Mutation von Weinberg, David V, Sieving, Paul A, Bingham, Eve L, Jampol, Lee M, Mets, Marilyn B

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