C. Van Hole

Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father Clinical variability of 22q11 deletion

Koenraad Devriendt, R. Van Hoestenberghe, C. Van Hole et al. · Clinical Genetics · 1997 · 79 citations

Life Sciences, Genetics, Molecular Genetics +13

Variability in expression of a familial 2.79 Mb microdeletion in chromosome14q22.1–22.2

Aimé Lumaka, C. Van Hole, Ingele Casteels et al. · American Journal of Medical Genetics Part A · 2012 · 22 citations

Life Sciences, Genetics, Molecular Genetics +17

Bilateral tibial agenesis with ectrodactyly (OMIM 119100): Further evidence for autosomal recessive inheritance

Ingrid Witters, Koenraad Devriendt, Ph. Moerman et al. · American Journal of Medical Genetics · 2001 · 19 citations · Full text

Medicine, Genetics, Pediatrics +16

Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entity.

Koenraad Devriendt, L Standaert, C. Van Hole et al. · Journal of Medical Genetics · 1998 · 12 citations · Full text

Medicine, Genetics, Pediatrics +14