D. V. Velzen

Fmr1 knockout mice: A model to study fragile X mental retardation

Guy Nagels, Rudi D'Hooge, Edwin Reyniers, 1994, Cell.

Mutations in the KCNQ 4 gene are responsible for autosomal dominant deafness in four DFNA 2 families

C. Cremers, P. Heyning, S. Bhasin, 1999 .

The full mutation in the FMR–1 gene of male fragile X patients is absent in their sperm

B. Oostra, J. Darby, A. Verkerk, 1993, Nature Genetics.

PCB PCB metabolites , chlorinated dioxins and furans in tissues of mustelids & om the Netherlands

D. V. Velzen, 2022 .

Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15.

R. Frants, P. Willems, D. van Velzen, 1995, Human molecular genetics.

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

G Van Camp, P Van de Heyning, C. Cremers, 1999, Human molecular genetics.

Fmr1 knockout mice: A model to study fragile X mental retardation

R. D'Hooge, G. Nagels, P. Cras, 1994, Cell.