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Journal Abstract Search

182 related items for PubMed ID: 23972321

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  • 2. A 7-year old female with arthrogryposis multiplex congenita, Duane retraction syndrome, and Marcus Gunn phenomenon due to a ZC4H2 gene mutation: a clinical presentation of the Wieacker-Wolff syndrome.
    Godfrey D, Torres A, Heidary G, Zahoor H, Lee A, Berry G, Engle E.
    Ophthalmic Genet; 2021 Oct; 42(5):612-614. PubMed ID: 33949289
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  • 7. Genotypic and phenotypic variability of 22q11.2 microduplications: An institutional experience.
    Yu A, Turbiville D, Xu F, Ray JW, Britt AD, Lupo PJ, Jain SK, Shattuck KE, Robinson SS, Dong J.
    Am J Med Genet A; 2019 Nov; 179(11):2178-2189. PubMed ID: 31479204
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  • 8. Familial Congenital Facial Synkinesis Due to 12q Duplication: A Case Report and Literature Review.
    Myers KA, Innes AM, Mah JK.
    Pediatrics; 2016 Dec; 138(6):. PubMed ID: 27940697
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  • 13. A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking phenomenon.
    Kaçar Bayram A, Per H, Quon J, Canpolat M, Ülgen E, Doğan H, Gumus H, Kumandas S, Bayram N, Bilguvar K, Çağlayan AO.
    Eur J Paediatr Neurol; 2015 Nov; 19(6):743-6. PubMed ID: 26190014
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  • 19. Marcus Gunn jaw winking synkinesis: report of two cases.
    Carman KB, Ozkan S, Yakut A, Ekici A.
    BMJ Case Rep; 2013 Jan 23; 2013():. PubMed ID: 23345532
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