H. Barth

Somatic Development in Children with Congenital Heart Defects

R. Lange, A. Lichtenberg, C. Vahl, 2018, The Journal of pediatrics.

Mitochondrial DNA m.3242G > A mutation, an under diagnosed cause of hypertrophic cardiomyopathy and renal tubular dysfunction?

Robert W. Taylor, R. Rodenburg, R. Wevers, 2012, European journal of medical genetics.

Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations

Stefan Mundlos, Denise Horn, Dirk Schnabel, 2006, Journal of Medical Genetics.

Cheyne‐Stokes respiration as an additional risk factor for pulmonary hypertension in a boy with trisomy 21 and atrioventricular septal defect

H. Barth, B. Hoch, 2001, Pediatric pulmonology.