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Nature Genetics, ISSN 1061-4036, 11/2013, Volume 45, Issue 11, pp. 1375 - 1381
Journal Article
by Fritsche, Lars and Igl, Wilmar and Cooke Bailey, Jessica N and Grassmann, Felix and Sengupta, Sebanti and Bragg-Gresham, Jennifer L and Burdon, K.P and Hebbring, Scott J and Wen, C and Gorski, Mathias and Kim, Ivana and Cho, D and Zack, D and Souied, Eric and Scholl, Henik and Bala, Elisa and ELee, K and Hunter, David and Sardell, R.J and Mitchell, Paul and Merriam, Joanna and Cipriani, Francesco and Hoffman, J.D and Schick, Tina and Lechanteur, Yara T. E and Guymer, Robyn and Johnson, Matthew and Jiang, Y and Stanton, Chloe and Buitendijk, Gabrielle and Zhan, Xiaowei and Kwong, A.M and Boleda, Alexis and Brooks, Matthew and Gieser, Linn and Ratna Priya, Rinki and Branham, Kari and Foerster, J.R and Heckenlively, John and Othman, Mohammad and Vote, Brendan J and Liang, H.H and Souzeau, Emmanuelle and McAllister, I.L and Isaacs, Timothy and Hall, J and Lake, S and Mackey, David and Constable, I.J and Craig, Jamie E and Kitchner, Terrie E and Yang, Z and Su, Z and Luo, H and Chen, D and Ouyang, H and Flagg, Ken and Lin, D and Mao, G and Ferreyra, Henry and Stark, Klaus and Strachwitz, Claudia and Wolf, A and Brandl, Caroline and Rudolph, G and Olden, Matthias and Morrison, Margaux and Morgan, Denise and Schu, Matthew and Ahn, J and Silvestri, Giuliana and Tsironi, Evangelia and Park, K.H and Farrer, Lindsay and Orlin, Anton and Brucker, A and Curcio, Christine A and Mohand-Sa'd, S and Sahel, José-Alain and Audo, Isabelle and Benchaboune, Mustapha and Cree, Angela and Rennie, C.A and Goverdhan, S.V and Grunin, Michelle and Hagbi-Levi, Shira and Campochiaro, Betsy and Katsanis, Nicholas and Holz, Frank and Blond, Frédéric and Blanché, H and Deleuze, J.-F and Igo, Robert and Truitt, Barbara and Peachey, Neal and Meuer, Stacy and Myers, Chelsea and Moore, E.L and Klein, Ronald and Hauser, Michael and ...
Nature Genetics, ISSN 1061-4036, 02/2016, Volume 48, Issue 2, pp. 134 - 143
Journal Article
Nature Genetics, ISSN 1061-4036, 2019, Volume 51, Issue 4, pp. 606 - 606
Journal Article
Genome Medicine, ISSN 1756-994X, 10/2013, Volume 5, Issue 9, pp. 84 - 84
Inherited retinal degenerative diseases (RDDs) display wide variation in their mode of inheritance, underlying genetic defects, age of onset, and phenotypic... 
INHERITED PHOTORECEPTOR DEGENERATIONS | LEBER CONGENITAL AMAUROSIS | HUMAN GENOME | RARE VARIANTS | EXOME CAPTURE | IDENTIFIES MUTATIONS | GENETICS & HEREDITY | COMPLEX DISEASES | LINKED RETINITIS-PIGMENTOSA | STRUCTURAL VARIATION | STATIONARY NIGHT BLINDNESS
Journal Article
Genetics, ISSN 0016-6731, 05/2017, Volume 206, Issue 1, pp. 119 - 133
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 11/2014, Volume 23, Issue 21, pp. 5827 - 5837
Journal Article
Journal Article