Literature DB >> 18671284

Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins.

Bettina Blaumeiser1, Barbara Oehl-Jaschkowitz, Wiktor Borozdin, Jürgen Kohlhase.   

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Year:  2008        PMID： 18671284     DOI： 10.1002/ajmg.a.32444

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  4 in total

1.  A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development.

Authors:  Xiuya Yu; Liyuan Hu; Xu Liu; Guodong Zhan; Mei Mei; Huijun Wang; Xiaohua Zhang; Zilong Qiu; Wenhao Zhou; Lin Yang
Journal:  Neurosci Bull       Date:  2018-05-21       Impact factor: 5.203

2.  Neurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2.

Authors:  E Fiori; L Babicola; D Andolina; A Coassin; T Pascucci; L Patella; Y-C Han; A Ventura; R Ventura
Journal:  Behav Genet       Date:  2015-05-31       Impact factor: 2.805

3.  A new variant of MYCN gene as a cause of Feingold syndrome.

Authors:  Naim Zeka; Ramush Bejiqi; Abdurrahim Gerguri; Leonore Zogaj; Haki Jashari
Journal:  Clin Case Rep       Date:  2022-05-23

4.  Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report.

Authors:  Magdalena Klaniewska; Krystian Toczewski; Anna Rozensztrauch; Michal Bloch; Agata Dzielendziak; Piotr Gasperowicz; Ryszard Slezak; Rafał Ploski; Małgorzata Rydzanicz; Robert Smigiel; Dariusz Patkowski
Journal:  Front Pediatr       Date:  2021-12-02       Impact factor: 3.418
  4 in total

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