L. Krols

Pure Familial Spastic Paraplegia: Clinical and Genetic Analysis of Nine Belgian Pedigrees

J. Weissenbach, C. Broeckhoven, J. Hazan, 1996, European journal of human genetics : EJHG.

On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family

C. Broeckhoven, J. Martín, J. Brucher, 2004, Acta Neuropathologica.

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.

J. Theuns, H. Backhovens, A. Wehnert, 1998, Human molecular genetics.

Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1–14.1

C. Broeckhoven, A. Dürr, A. Brice, 1997, Human Genetics.

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

J. Weissenbach, Y. Agid, C. Broeckhoven, 1995, Nature Genetics.

Report of the sixth international workshop on human chromosome 3 mapping 1995.

A. Jonasdottir, S. Naylor, M. Grompe, 1994, Cytogenetics and cell genetics.