Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 1
1967 1
1968 1
1972 1
1976 3
1977 2
1978 3
1980 1
1981 4
1982 1
1983 2
1984 2
1985 2
1986 6
1987 3
1988 5
1989 8
1990 4
1991 4
1992 5
1993 7
1994 4
1995 4
1996 2
1997 7
1998 10
1999 7
2000 11
2001 6
2002 4
2003 7
2004 10
2005 12
2006 1
2007 8
2008 7
2009 6
2010 7
2011 9
2012 8
2013 5
2014 3
2015 5
2016 21
2017 6
2018 13
2019 7
2020 7
2021 8
2022 5
2023 3
2024 2
2025 2

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

258 results

Results by year

Filters applied: . Clear all
Page 1
Nonsyndromic Retinitis Pigmentosa Overview.
Fahim AT, Daiger SP, Weleber RG. Fahim AT, et al. Among authors: weleber rg. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301590 Free Books & Documents. Review.
Bietti Crystalline Dystrophy.
Vargas M, Mitchell A, Yang P, Weleber R. Vargas M, et al. Among authors: weleber r. 2012 Apr 12 [updated 2019 Feb 7]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2012 Apr 12 [updated 2019 Feb 7]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 22497028 Free Books & Documents. Review.
Stargardt's macular dystrophy.
Weleber RG. Weleber RG. Arch Ophthalmol. 1994 Jun;112(6):752-4. doi: 10.1001/archopht.1994.01090180050033. Arch Ophthalmol. 1994. PMID: 8002831 No abstract available.
Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy Overview.
Kumaran N, Pennesi ME, Yang P, Trzupek KM, Schlechter C, Moore AT, Weleber RG, Michaelides M. Kumaran N, et al. Among authors: weleber rg. 2018 Oct 4 [updated 2023 Mar 23]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2018 Oct 4 [updated 2023 Mar 23]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 30285347 Free Books & Documents. Review.
Functional evaluation in inherited retinal disease.
Daich Varela M, Georgiou M, Hashem SA, Weleber RG, Michaelides M. Daich Varela M, et al. Among authors: weleber rg. Br J Ophthalmol. 2022 Nov;106(11):1479-1487. doi: 10.1136/bjophthalmol-2021-319994. Epub 2021 Nov 25. Br J Ophthalmol. 2022. PMID: 34824084 Review.
Ruvalcaba-Myhre-Smith syndrome.
Gretzula JC, Hevia O, Schachner LS, DiLiberti JH, Ruvalcaba RH, Schimschock JR, Weleber RG, Halal F, Lipson MH, Blumberg B, et al. Gretzula JC, et al. Among authors: weleber rg. Pediatr Dermatol. 1988 Feb;5(1):28-32. doi: 10.1111/j.1525-1470.1988.tb00880.x. Pediatr Dermatol. 1988. PMID: 3380760
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, Balousha G, Benedicenti F, Birch D, Bitoun P, Blain D, Bocquet B, Branham K, Català-Mora J, De Baere E, Dollfus H, Falana M, Giorda R, Golovleva I, Gottlob I, Heckenlively JR, Jacobson SG, Jones K, Jägle H, Janecke AR, Kellner U, Liskova P, Lorenz B, Martorell-Sampol L, Messias A, Meunier I, Belga Ottoni Porto F, Papageorgiou E, Plomp AS, de Ravel TJL, Reiff CM, Renner AB, Rosenberg T, Rudolph G, Salati R, Sener EC, Sieving PA, Stanzial F, Traboulsi EI, Tsang SH, Varsanyi B, Weleber RG, Zobor D, Stingl K, Wissinger B, Kohl S. Solaki M, et al. Among authors: weleber rg. Hum Mutat. 2022 Jul;43(7):832-858. doi: 10.1002/humu.24371. Epub 2022 Apr 14. Hum Mutat. 2022. PMID: 35332618 Review.
Chromosome anomalies.
Hecht F, Weleber RG, Giblett ER. Hecht F, et al. Among authors: weleber rg. Lancet. 1967 Apr 15;1(7494):848. doi: 10.1016/s0140-6736(67)92816-4. Lancet. 1967. PMID: 4164314 No abstract available.
258 results