- CiteSeerX 10.1.1.461.5915. doi:10.1126/science.2937147. PMID 2937147.
Weleber RG (June 2002). "Infantile and
childhood retinal blindness: a molecular...
- Weissenbacher–Zweymuller
syndrome Welander distal myopathy,
Swedish type
Weleber–Hecht–Bigley
syndrome Wellesley–Carmen–French
syndrome Wells–Jankovic syndrome...
- ****ociation. 2015-12-18. "Bardet-Biedl (Laurence Moon)". Adamus, G., Ren, G. &
Weleber, R.G.
Autoantibodies against retinal proteins in
paraneoplastic and autoimmune...
- C M; Maumenee, I H; Lewis, R A; Hejtmancik, J F; Litt, M; Lovrien, E;
Weleber, R; Bachynski, B; Zwas, F; Klingaman, R; Fishman, G (1989). "Molecular...
- PMID 3014804. Roberts, MF; Fishman, GA; Roberts, DK; Heckenlively, JR;
Weleber, RG; Anderson, RJ; Grover, S (June 2002). "Retrospective, longitudinal...
- the kidney) were
features of the syndrome. A
recent article by
Beals and
Weleber (2007) also
noted that a
majority of
patients also have
small capital femoral...
- 107834. doi:10.1016/j.exer.2019.107834. PMID 31639339.
Kumaran N,
Moore AT,
Weleber RG,
Michaelides M (September 2017). "Leber
congenital amaurosis/early-onset...
- ucdavis.edu.
Retrieved 11
October 2022.
Boycott KM,
Pearce WG,
Musarella MA,
Weleber RG,
Maybaum TA,
Birch DG, et al. (April 1998). "Evidence for
genetic heterogeneity...
- Hamasaki, D.; Kubota, S.; Sakuma, H.; An, W.; Fujimaki, T.; McLaren, M. J.;
Weleber, R. G.; Inana, G. (2000). "HRG4 (UNC119)
mutation found in cone-rod dystrophy...
-
complete congenital stationary night blindness was
provided by
Richard G.
Weleber at the
University of
Alberta in 2000. The NYX gene is
located on the short...
