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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2003 | 1 |
2008 | 1 |
2023 | 1 |
2024 | 1 |
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Craniofacial-deafness-hand syndrome revisited.
Am J Med Genet A. 2003 Nov 15;123A(1):91-4. doi: 10.1002/ajmg.a.20501.
Am J Med Genet A. 2003.
PMID: 14556253
Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome?
Gad A, Laurino M, Maravilla KR, Matsushita M, Raskind WH.
Gad A, et al.
Am J Med Genet A. 2008 Jul 15;146A(14):1880-5. doi: 10.1002/ajmg.a.32402.
Am J Med Genet A. 2008.
PMID: 18553554
Free PMC article.
In addition, mutations in PAX3 have been found in WS type 3 that is distinguished by musculoskeletal abnormalities, and in a family with a rare subtype of WS, craniofacial-deafness-hand syndrome (CDHS), characterized by dysmorphic facial features, hand …
In addition, mutations in PAX3 have been found in WS type 3 that is distinguished by musculoskeletal abnormalities, and in a family with a r …
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Disentangling the complex landscape of sleep-wake disorders with data-driven phenotyping: A study of the Bernese center.
Aellen FM, Van der Meer J, Dietmann A, Schmidt M, Bassetti CLA, Tzovara A.
Aellen FM, et al.
Eur J Neurol. 2024 Jan;31(1):e16026. doi: 10.1111/ene.16026. Epub 2023 Aug 13.
Eur J Neurol. 2024.
PMID: 37531449
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