Search filters

List of works by Suzanne C E H Sallevelt

A comprehensive strategy for exome-based preconception carrier screening.

scientific article published on 27 October 2016

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

scientific article published on 01 September 2019

De novo mtDNA point mutations are common and have a low recurrence risk.

scientific article

Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease.

scientific article published on 13 February 2018

Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck

scientific article published on 5 January 2016

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

article

Paulina is supported by:

About Paulina

Help