Emiel Baten

Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E

Eva Klopocki, Bianca P. Hennig, Katarina Dathe et al. · The American Journal of Human Genetics · 2010 · 144 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

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

2q31.1 microdeletion syndrome: redefining the associated clinical phenotype

Boyan Dimitrov, Irina Balikova, Thomy de Ravel et al. · Journal of Medical Genetics · 2010 · 67 citations

Life Sciences, Genetics, Molecular Genetics +16

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

The facio-audio-symphalangism syndrome in a four generation family with a nonsense mutation in the NOG-gene

J.J. van den Ende, Paul Mattelaer, Frank Declau et al. · Clinical Dysmorphology · 2005 · 22 citations

Medicine, Genetics, Molecular Genetics +15