Publications by authors named "V Vernimmen"

Claim this Profile
R
Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with point variants.
Laurence Pacot, Marinus Blok, Dominique Vidaud, Laura Fertitta, Ingrid Laurendeau, Vivian Vernimmen

J Med Genet· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Preimplantation genetic testing for neurofibromatosis type 1: molecular genetic aspects and impact on reproductive counseling.
V Vernimmen, M De Rycke, C Moutou, J Dreesen, M J Blok

Hum Reprod· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes.
Dmitrijs Rots, Sanaa Choufani, Victor Faundes, Alexander J M Dingemans, Shelagh Joss, Vivian Vernimmen

Am J Hum Genet· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Preimplantation genetic testing for Neurofibromatosis type 1: more than 20 years of clinical experience.
Vivian Vernimmen, Aimée D C Paulussen, Jos C F M Dreesen, Ron J van Golde, Masoud Zamani Esteki

Eur J Hum Genet· August 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience.
Brigitte H W Faas, Dineke Westra, Sonja A de Munnik, Maartje van Rij, Carlo Marcelis, Vivian Vernimmen

Prenat Diagn· April 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis