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

Am J Med Genet A. 2016 Jan;170A(1):283-4. doi: 10.1002/ajmg.a.37416. Epub 2015 Oct 8.

Authors

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

Affiliations

¹ Institute of Human Genetics, University Hospital, RWTH, Aachen, Germany.
² Childreńs Hospital, University of Tübingen, Tübingen, Germany.

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

No abstract available

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

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Beckwith-Wiedemann Syndrome / genetics*
Chromosomes, Human, Pair 11 / genetics*
Fetal Growth Retardation / genetics*
Genetic Testing
Genomic Imprinting / genetics
Humans
Insulin-Like Growth Factor II / genetics*

Substances

IGF2 protein, human
Insulin-Like Growth Factor II