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List of works by Mark J Hamilton

Brain Structural Features of Myotonic Dystrophy Type 1 and their Relationship with CTG Repeats

scientific article published on 01 January 2019

CDK13-related disorder

scientific article published on 11 December 2018

Chromosomal microarray analysis for looked after children: a double-edged sword?

scientific article published on 26 September 2014

De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1

scientific article published on 02 July 2018

Elevated plasma levels of cardiac troponin-I predict left ventricular systolic dysfunction in patients with myotonic dystrophy type 1: A multicentre cohort follow-up study

scientific article

Growing up with spinal muscular atrophy with respiratory distress (SMARD1).

scientific article published on 22 October 2014

Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.

scientific article

Outcome Measures for Central Nervous System Evaluation in Myotonic Dystrophy Type 1 May Be Confounded by Deficits in Motor Function or Insight

scientific article published on 02 October 2018

Phenotypes of 8q13.2-q13.3 microdeletion: Case report and literature review of an emerging recurrent microdeletion syndrome

scientific article published on 10 December 2015

Rubinstein-Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrum

scientific article published on 26 July 2016

The prevalence of faecal incontinence in myotonic dystrophy type 1

scientific article published on 07 June 2019

Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1

scientific article published on 12 August 2020

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