S. Lindquist

Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease

P. Johannsen, B. B. Andersen, H. Braendgaard, 2013, Clinical genetics.

Genetic testing in familial AD and FTD: Mutation and phenotype spectrum in a Danish cohort

G. Waldemar, M. Batbayli, SG Lindquist, 2009, Clinical genetics.

Further delineation of the 22q13 deletion syndrome

C. Lundsteen, N. Tommerup, M. Kirchhoff, 2005, Clinical dysmorphology.

Deletion of CUL4B leads to concordant phenotype in a monozygotic twin pair

Z. Tümer, K. Ravn, K. Nielsen, 2012, Clinical genetics.