Exclusion of the human collagen type XVII (COL17A1) gene as the cause of Thiel-Behnke corneal dystrophy (CDB2) on chromosome 10q23-q25

By Sullivan Lori S.   Zhao Xinping   Bowne Sara J.   Xu Xiangyang   Daiger Stephen P.   Yee Steven B.   Yee Richard W.  

Current Eye Research, Vol. 27, Iss. 4, 2003-10 ,pp. : 223-226

Informa Healthcare

Access to resources Recommend Favorite

Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss

By Chinetti Viviana   Iossa Sandra   Auletta Gennaro   Laria Carla   de Luca Maria   Leva Francesca Di   Riccardi Pasquale   Giannini Pasquale   Gasparini Paolo   Ciccodicola Alfredo   Marciano Elio   Franzè Annamaria  

International Journal of Audiology, Vol. 49, Iss. 4, 2010-03 ,pp. : 326-331

Informa Healthcare

Access to resources Recommend Favorite

Opponent-color models and the influence of rod signals on the loci of unique hues

By Buck S.L.   Knight R.F.   Bechtold J.  

Vision Research, Vol. 40, Iss. 24, 2000-10 ,pp. : 3333-3344

Elsevier

Access to resources Recommend Favorite

Exclusion of the apoE gene in autosomal dominant retinitis pigmentosa

By Souied E.H.   Benlian P.   Rozet J.-M.   Gerber S.   Lagarde J.-P.   Coscas G.   Soubrane G.   Duffier J.-L.   Munnich A.   Kaplan J.  

Vision Research, Vol. 38, Iss. 24, 1998-12 ,pp. : 3829-3831

Elsevier

Access to resources Recommend Favorite

Pseudo-Vitelliform Macular Detachment and Cuticular Drusen: Exclusion of 6 Candidate Genes

By Barbazetto Irene   Yannuzzi Nicolas   Klais Christina   Merriam Joanna   Zernant Jana   Peiretti Enrico   Yannuzzi Lawrence   Allikmets Rando  

Ophthalmic Genetics, Vol. 28, Iss. 4, 2007-10 ,pp. : 192-197

Informa Healthcare

Access to resources Recommend Favorite