Detection of the XbaI RFLP within the retinoblastoma locus by PCR

gan McGee, Terri L., Cowley, Glenn S., Yandell, David W., Dryja, Thaddeus P.
Cyhoeddwyd 1990

Low prevalence of LRAT mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa

gan Sweeney, Meredith O., McGee, Terri L., Berson, Eliot L., Dryja, Thaddeus P.
Cyhoeddwyd 2007

Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa

gan McGee, Terri L., Seyedahmadi, Babak Jian, Sweeney, Meredith O., Dryja, Thaddeus P., Berson, Eliot L.
Cyhoeddwyd 2010

Disease Course in Patients with Autosomal Recessive Retinitis Pigmentosa due to the USH2A Gene

gan Sandberg, Michael A., Rosner, Bernard, Weigel-DiFranco, Carol, McGee, Terri L., Dryja, Thaddeus P., Berson, Eliot L.
Cyhoeddwyd 2008

A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance

gan Rio Frio, Thomas, McGee, Terri L., Wade, Nicholas M., Iseli, Christian, Beckmann, Jacques S., Berson, Eliot L., Rivolta, Carlo
Cyhoeddwyd 2009

Null RPGRIP1 Alleles in Patients with Leber Congenital Amaurosis

gan Dryja, Thaddeus P., Adams, Scott M., Grimsby, Jonna L., McGee, Terri L., Hong, Dong-Hyun, Li, Tiansen, Andréasson, Sten, Berson, Eliot L.
Cyhoeddwyd 2001

A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa

gan den Hollander, Anneke I., McGee, Terri L., Ziviello, Carmela, Banfi, Sandro, Dryja, Thaddeus P., Gonzalez-Fernandez, Federico, Ghosh, Debashis, Berson, Eliot L.
Cyhoeddwyd 2008

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

gan Dryja, Thaddeus P., McGee, Terri L., Berson, Eliot L., Fishman, Gerald A., Sandberg, Michael A., Alexander, Kenneth R., Derlacki, Deborah J., Rajagopalan, Aruna S.
Cyhoeddwyd 2005

Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutation

gan Hartong, Dyonne T., McGee, Terri L., Sandberg, Michael A., Berson, Eliot L., Asselbergs, Folkert W., van der Harst, Pim, De Vivo, Immaculata, Dryja, Thaddeus P.
Cyhoeddwyd 2009

AAV-mediated RLBP1 gene therapy improves the rate of dark adaptation in Rlbp1 knockout mice

gan Choi, Vivian W, Bigelow, Chad E, McGee, Terri L, Gujar, Akshata N, Li, Hui, Hanks, Shawn M, Vrouvlianis, Joanna, Maker, Michael, Leehy, Barrett, Zhang, Yiqin, Aranda, Jorge, Bounoutas, George, Demirs, John T, Yang, Junzheng, Ornberg, Richard, Wang, Yu, Martin, Wendy, Stout, Kelly R, Argentieri, Gregory, Grosenstein, Paul, Diaz, Danielle, Turner, Oliver, Jaffee, Bruce D, Police, Seshidhar R, Dryja, Thaddeus P
Cyhoeddwyd yn Mol Ther Methods Clin Dev (2015)