Feenstra, I.

Update Persondata

• chromosome
• gene
• mutations
• screening

Publications

(the most recent at the top)

A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsy

A de novo microdeletion in chromosome 8q12.3q13.2: association with mild intellectual disability and epilepsy?

Genetic syndromes and the autism spectrum

Autisme en genetische syndromen

Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6

All publications..