Bert Ba de Vries

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

Bert Ba de Vries, J. P. Fryns, Merlin G. Butler et al. · Journal of Medical Genetics · 1993 · 93 citations · Full text

A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology

Eugenia Migliavacca, Christelle Golzio, Katrin Männik et al. · The American Journal of Human Genetics · 2015 · 71 citations · Full text

Clinical Disorders, Ciliary Dysfunction, Disease Pathophysiology +7

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications

Josephine Wincent, Damien L. Bruno, Bregje W.M. van Bon et al. · Molecular Syndromology · 2010 · 36 citations · Full text

Distal 22Q11.2, Developmental Anomaly, Urology +11

The epileptology of Koolen‐de Vries syndrome: Electro‐clinico‐radiologic findings in 31 patients

Kenneth A. Myers, Simone Mandelstam, Georgia Ramantani et al. · Epilepsia · 2017 · 32 citations · Full text

DNA testing for fragile X syndrome: implications for parents and family.

M A van Rijn, Bert Ba de Vries, Aad Tibben et al. · Journal of Medical Genetics · 1997 · 23 citations · Full text