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 NCBI Filters

Results by year

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

Year Number of Results
1946 1
1947 1
1948 1
1951 2
1952 4
1953 1
1956 1
1957 2
1959 3
1960 4
1961 7
1962 6
1963 2
1964 7
1965 10
1966 4
1967 10
1968 12
1969 10
1970 10
1971 23
1972 14
1973 4
1974 7
1975 12
1976 2
1977 10
1978 11
1979 15
1980 16
1981 9
1982 9
1983 9
1984 12
1985 6
1986 8
1987 8
1988 5
1989 6
1990 9
1991 12
1992 27
1993 26
1994 29
1995 34
1996 28
1997 25
1998 31
1999 22
2000 37
2001 36
2002 17
2003 26
2004 18
2005 16
2006 34
2007 23
2008 26
2009 23
2010 29
2011 35
2012 40
2013 34
2014 29
2015 48
2016 36
2017 47
2018 46
2019 45
2020 57
2021 53
2022 41
2023 40
2024 17

Text availability

Article attribute

Article type

Publication date

Search Results

1,294 results

Results by year

Filters applied: . Clear all
Page 1
Review and update of mutations causing Waardenburg syndrome.
Pingault V, Ente D, Dastot-Le Moal F, Goossens M, Marlin S, Bondurand N. Pingault V, et al. Hum Mutat. 2010 Apr;31(4):391-406. doi: 10.1002/humu.21211. Hum Mutat. 2010. PMID: 20127975 Free article. Review.
Waardenburg syndrome (WS) is characterized by the association of pigmentation abnormalities, including depigmented patches of the skin and hair, vivid blue eyes or heterochromia irides, and sensorineural hearing loss. However, other features such as dystopia canthor …
Waardenburg syndrome (WS) is characterized by the association of pigmentation abnormalities, including depigmented patches of …
Waardenburg syndrome.
Read AP, Newton VE. Read AP, et al. J Med Genet. 1997 Aug;34(8):656-65. doi: 10.1136/jmg.34.8.656. J Med Genet. 1997. PMID: 9279758 Free PMC article. Review.
Type III WS (Klein-Waardenburg syndrome, with abnormalities of the arms) is an extreme presentation of type I; some but not all patients are homozygotes. Type IV WS (Shah-Waardenburg syndrome with Hirschsprung disease) can be caused by mutations in the …
Type III WS (Klein-Waardenburg syndrome, with abnormalities of the arms) is an extreme presentation of type I; some but not al …
Waardenburg syndrome.
Dourmishev AL, Dourmishev LA, Schwartz RA, Janniger CK. Dourmishev AL, et al. Int J Dermatol. 1999 Sep;38(9):656-63. doi: 10.1046/j.1365-4362.1999.00750.x. Int J Dermatol. 1999. PMID: 10517681 Review. No abstract available.
Waardenburg Syndrome Type 1.
Agrawal R, Walia S. Agrawal R, et al. Indian J Ophthalmol. 2022 Jul;70(7):2679-2681. doi: 10.4103/ijo.IJO_3003_21. Indian J Ophthalmol. 2022. PMID: 35791202 Free PMC article. No abstract available.
[Waardenburg syndrome].
Boubekri A, Atmani W, Bensghir M. Boubekri A, et al. Rev Prat. 2023 Dec;73(10):1106. Rev Prat. 2023. PMID: 38294479 French. No abstract available.
Waardenburg syndrome.
Read AP. Read AP. Adv Otorhinolaryngol. 2000;56:32-8. doi: 10.1159/000059069. Adv Otorhinolaryngol. 2000. PMID: 10868211 Review. No abstract available.
Waardenburg syndrome type 1 with unilateral glaucoma.
Kavitha S, Gopalakrishna M. Kavitha S, et al. Indian J Med Res. 2022 Jul;156(1):161. doi: 10.4103/ijmr.IJMR_2594_20. Indian J Med Res. 2022. PMID: 36510911 Free PMC article. No abstract available.
Waardenburg Syndrome Type I.
Gowda VK, Srinivas S, Srinivasan VM. Gowda VK, et al. Indian J Pediatr. 2020 Mar;87(3):244. doi: 10.1007/s12098-019-03170-5. Epub 2020 Jan 27. Indian J Pediatr. 2020. PMID: 31989460 No abstract available.
Shah-Waardenburg syndrome.
Mahmoudi A, Rami M, Khattala K, Elmadi A, Afifi MA, Youssef B. Mahmoudi A, et al. Pan Afr Med J. 2013;14:60. doi: 10.11604/pamj.2013.14.60.1543. Epub 2013 Feb 12. Pan Afr Med J. 2013. PMID: 23565307 Free PMC article.
Shah-Waardenburg syndrome (SWS) is a neurocristopathy and is characterized by Hirschsprung's disease (HD), deafness, and depigmentation of hairs, skin, and iris. Is a very rare congenital disorder with variable clinical expression. This report describes a 4-day-old …
Shah-Waardenburg syndrome (SWS) is a neurocristopathy and is characterized by Hirschsprung's disease (HD), deafness, and depig …
Waardenburg syndrome.
Bist J, Adhikari P, Sharma AK. Bist J, et al. Clin Exp Optom. 2011 Mar;94(2):240-2. doi: 10.1111/j.1444-0938.2010.00533.x. Epub 2010 Oct 29. Clin Exp Optom. 2011. PMID: 21352370 Free article. No abstract available.
1,294 results

Searches related to "waardenburg syndrome"