JP Fryns

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

Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences

Emiel Baten, JP Fryns, Koenraad Devriendt · Clinical Genetics · 2002 · 76 citations

Life Sciences, Genetics, Cytogenetics +16

A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy

Jean Steyaert, Susan Umans, D Willekens et al. · Clinical Genetics · 1997 · 72 citations

Medicine, Psychiatry, Psychology +15

Neuropathological findings in Moebius syndrome

Martin Lammens, Ph. Moerman, JP Fryns et al. · Clinical Genetics · 1998 · 42 citations

Medicine, Neurology, Neuroscience +17