Lieve Standaert

Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes

Frauke Coppieters, Ingele Casteels, Françoise Meire et al. · Human Mutation · 2010 · 146 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the Branchio-Oto-Renal syndrome. A family study

Chr. Stinckens, Lieve Standaert, Jan Casselman et al. · International Journal of Pediatric Otorhinolaryngology · 2001 · 60 citations

Medicine, Neurology, Otolaryngology +15

Cohen syndrome: the clinical symptoms and stigmata at a young age

Jean‐Pierre Fryns, Eric Legius, Koenraad Devriendt et al. · Clinical Genetics · 1996 · 42 citations

Medicine, Child Health, Pediatrics +17

Otological Manifestations of Charge Association

Ingeborg Dhooge, Lieve Standaert, Mark Lemmerling et al. · Annals of Otology Rhinology & Laryngology · 1998 · 38 citations

Health Professions, Otolaryngology, Radiology +17

Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis

Françoise Meire, Lieve Standaert, J. J. De Laey et al. · American Journal of Medical Genetics · 1987 · 30 citations

Medicine, Neurology, Pediatric Neurology +4