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

Year Number of Results
1951 2
1952 2
1960 3
1961 3
1962 5
1963 2
1964 3
1965 4
1966 1
1967 1
1969 1
1970 2
1971 2
1972 2
1974 1
1977 1
1978 3
1980 2
1981 2
1984 1
1986 3
1988 1
1989 1
1991 1
1992 1
1993 2
1994 1
1996 4
1997 1
1998 1
1999 2
2000 2
2001 2
2002 1
2003 2
2005 1
2010 3
2011 4
2012 1
2013 4
2014 1
2015 1
2016 2
2017 2
2018 2
2019 2
2020 2
2021 1
2022 2
2024 0

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90 results

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Page 1
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 Type I.
Milunsky JM. Milunsky JM. 2001 Jul 30 [updated 2022 Oct 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2001 Jul 30 [updated 2022 Oct 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301703 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Waardenburg syndrome type I (WS1) is an auditory-pigmentary disorder comprising congenital sensorineural hearing loss and pigmentary disturbances of the iris, hair, and skin along with dystopia canthorum (lateral displacement of the inner c …
CLINICAL CHARACTERISTICS: Waardenburg syndrome type I (WS1) is an auditory-pigmentary disorder comprising congenital sensorine …
Heterogeneity in Waardenburg syndrome.
Hageman MJ, Delleman JW. Hageman MJ, et al. Am J Hum Genet. 1977 Sep;29(5):468-85. Am J Hum Genet. 1977. PMID: 331943 Free PMC article. Review.
Heterogeneity of Waardenburg syndrome is demonstrated in a review of 1,285 patients from the literature and 34 previously unreported patients in five families in the Netherlands. The syndrome seems to consist of two genetically distinct entities that can be d …
Heterogeneity of Waardenburg syndrome is demonstrated in a review of 1,285 patients from the literature and 34 previously unre …
Waardenburg's syndrome.
AASVED H. AASVED H. Acta Ophthalmol (Copenh). 1962;40:622-8. doi: 10.1111/j.1755-3768.1962.tb07838.x. Acta Ophthalmol (Copenh). 1962. PMID: 14010515 No abstract available.
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.
PARTINGTON MW. PARTINGTON MW. Can Med Assoc J. 1964 Apr 25;90(17):1008-17. Can Med Assoc J. 1964. PMID: 14166458 Free PMC article.
Waardenburg's syndrome consists of lateral displacement of the inner canthi of the eyes (dystopia canthorum), a broad nasal root and confluent eyebrows, heterochromia iridum, a white forelock and congenital deafness. ...The interocular dimensions of the remai …
Waardenburg's syndrome consists of lateral displacement of the inner canthi of the eyes (dystopia canthorum), a broad n …
Waardenburg syndrome.
Lee D, Lanza J, Har-El G. Lee D, et al. Otolaryngol Head Neck Surg. 1996 Jan;114(1):166-7. doi: 10.1016/S0194-59989670306-6. Otolaryngol Head Neck Surg. 1996. PMID: 8570242 No abstract available.
Waardenburg's syndrome.
CALINIKOS J. CALINIKOS J. J Laryngol Otol. 1963 Jan;77:59-62. doi: 10.1017/s0022215100060369. J Laryngol Otol. 1963. PMID: 14017880 No abstract available.
Waardenburg's syndrome.
GHOSH S. GHOSH S. Indian J Child Health. 1962 Sep;11:448-9. Indian J Child Health. 1962. PMID: 13947542 No abstract available.
Waardenburg's syndrome.
Poche GW, Christianson HB. Poche GW, et al. Cutis. 1978 May;21(5):685-6. Cutis. 1978. PMID: 417897 No abstract available.
90 results