N. Schaub

Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- and A/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)

L. Terracciano, P. Demougin, C. Noppen, 2011, PloS one.

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome

K. Heinimann, P. Miny, S. Buechner, 2004, Journal of Medical Genetics.

Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?

P. Itin, K. Heinimann, B. Burger, 2011, The oncologist.

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome

K. Heinimann, P. Miny, S. Buechner, 2004, Journal of Medical Genetics.

Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?

P. Itin, K. Heinimann, B. Burger, 2011, The oncologist.