Griet Van Buggenhout

Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

Jacopo Celli, Pascal H. G. Duijf, Ben C.J. Hamel et al. · Cell · 1999 · 715 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

Femke Hannes, Andrew J. Sharp, Heather C. Mefford et al. · Journal of Medical Genetics · 2008 · 346 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)

Nicole Maas, Griet Van Buggenhout, Femke Hannes et al. · Journal of Medical Genetics · 2007 · 178 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients

Griet Van Buggenhout, Conny M.A. van Ravenswaaij‐Arts, Nicole Maas et al. · European Journal of Medical Genetics · 2005 · 137 citations

Life Sciences, Genetics, Molecular Genetics +14

Structural chromosome rearrangements in couples with recurrent fetal wastage

Jean‐Pierre Fryns, Griet Van Buggenhout · European Journal of Obstetrics & Gynecology and Reproductive Biology · 1998 · 129 citations

Life Sciences, Genetics, Molecular Genetics +13