Adams Oliver syndrome with cerebellar cortical dysplasia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/article/10.1007/s00381-018-3810-1/fulltext.html
Reference5 articles.
1. Whitley CB, Gorlin RJ (1991) Adams-Oliver syndrome revisited. Am J Med Genet 40:319–326. https://doi.org/10.1002/ajmg.1320400315
2. Hassed S, Li S, Mulvihill J, Aston C, Palmer S (2017) Adams-Oliver syndrome review of the literature: refining the diagnostic phenotype. Am J Med Genet A 173:790–800. https://doi.org/10.1002/ajmg.a.37889
3. Nohata N, Uchida Y, Stratman AN, Adams RH, Zheng Y et al (2016) Temporal-specific roles of Rac1 during vascular development and retinal angiogenesis. Dev Biol 411:183–194. https://doi.org/10.1016/j.ydbio.2016.02.005
4. Pérez-García C, Martín YR, Del Hoyo AA, Rodríguez CM, Domínguez MC (2017) Adams-Oliver syndrome with unusual central nervous system findings and an extrahepatic portosystemic shunt. Pediatr Rep 9:7211. https://doi.org/10.4081/pr.2017.7211
5. D’Amico A, Melis D, D’Arco F, Di Paolo N, Carotenuto B et al (2013) Adams Oliver syndrome: description of a new phenotype with cerebellar abnormalities in a family. Pol J Radiol 78:83–87. https://doi.org/10.12659/PJR.889531
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1. Using whole exome sequencing to identify susceptibility genes associated with nonsyndromic cleft lip with or without cleft palate;Molecular Genetics and Genomics;2022-11-02
2. Expanding the phenotype in Adams–Oliver syndrome correlating with the genotype;American Journal of Medical Genetics Part A;2019-10-25
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