Literature DB >> 26447000

No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders.

Anne Müller1, Lukas Soellner1, Gerhard Binder2, Matthias Begemann1, Thomas Eggermann1.   

Abstract

Entities:  

Keywords:  Beckwith-Wiedemann syndrome; IGF2 mutations; Silver-Russell syndrome

Mesh：

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Year:  2015        PMID： 26447000     DOI： 10.1002/ajmg.a.37416

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


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  2 in total

1.  Diagnosis and management of Silver-Russell syndrome: first international consensus statement.

Authors:  Emma L Wakeling; Frédéric Brioude; Oluwakemi Lokulo-Sodipe; Susan M O'Connell; Jennifer Salem; Jet Bliek; Ana P M Canton; Krystyna H Chrzanowska; Justin H Davies; Renuka P Dias; Béatrice Dubern; Miriam Elbracht; Eloise Giabicani; Adda Grimberg; Karen Grønskov; Anita C S Hokken-Koelega; Alexander A Jorge; Masayo Kagami; Agnes Linglart; Mohamad Maghnie; Klaus Mohnike; David Monk; Gudrun E Moore; Philip G Murray; Tsutomu Ogata; Isabelle Oliver Petit; Silvia Russo; Edith Said; Meropi Toumba; Zeynep Tümer; Gerhard Binder; Thomas Eggermann; Madeleine D Harbison; I Karen Temple; Deborah J G Mackay; Irène Netchine
Journal:  Nat Rev Endocrinol       Date:  2016-09-02       Impact factor: 43.330

2.  De Novo Mutation of Paternal IGF2 Gene Causing Silver-Russell Syndrome in a Sporadic Patient.

Authors:  Deguo Liu; Yajian Wang; Xiu-An Yang; Deyun Liu
Journal:  Front Genet       Date:  2017-08-08       Impact factor: 4.599
  2 in total

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