Article info
Neurological rarities
Gordon Holmes syndrome: finally genotype meets phenotype
- Correspondence to Professor Marios Hadjivassiliou, Academic Department of Neurosciences, Royal Hallamshire Hospital, Glossop Road, Sheffield S10 2JF, UK; m.hadjivassiliou{at}sheffield.ac.uk
Citation
Gordon Holmes syndrome: finally genotype meets phenotype
Publication history
- Accepted September 1, 2017
- First published September 28, 2017.
Online issue publication
January 08, 2018
Article Versions
- Previous version (8 January 2018).
- Previous version (8 January 2018).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.
Other content recommended for you
- Clinical and genetic spectrum of RNF216-related disorder: a new case and literature review
- Phenotypic spectrum of POLR3B mutations: isolated hypogonadotropic hypogonadism without neurological or dental anomalies
- A novel mutation in RNF216 gene in an Indian case with Gordon Holmes syndrome
- Rare case of Gordon Holmes syndrome
- Idiopathic hypogonadotropic hypogonadism reversal after testosterone replacement in a 34-year-old male
- Adult-onset reversible idiopathic hypogonadotropic hypogonadism in male adult carrying a WDR11 missense mutation
- The effects of opioids on the endocrine system: an overview
- Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes
- Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1
- Hypogonadism evaluation: clinical examination is the key