Detection of the XbaI RFLP within the retinoblastoma locus by PCR

por McGee, Terri L., Cowley, Glenn S., Yandell, David W., Dryja, Thaddeus P.
Publicado 1990

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

por Sweeney, Meredith O., McGee, Terri L., Berson, Eliot L., Dryja, Thaddeus P.
Publicado 2007

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

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

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

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

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

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

Null RPGRIP1 Alleles in Patients with Leber Congenital Amaurosis

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

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

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

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

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

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

por 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.
Publicado 2009

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

por 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
Publicado en Mol Ther Methods Clin Dev (2015)