Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome

Silver-Russell syndrome (SRS) is characterized by pre- and postnatal growth failure and other dysmorphic features. The syndrome is genetically heterogenous, but maternal uniparental disomy of chromosome 7 has been demonstrated in ∼7% of cases. This suggests that at least one gene on chromosome 7 is...

Full description

Saved in:
Bibliographic Details
Main Authors: Monk, David, Wakeling, Emma L, Proud, Virginia, Hitchins, Megan, Abu-Amero, Sayeda N., Stanier, Philip, Preece, Michael A., Moore, Gudrun E
Format: Artigo
Language:Inglês
Published: The American Society of Human Genetics 2000
Subjects:
Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1288348/
https://ncbi.nlm.nih.gov/pubmed/10631135
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items