L. Born

发表

ABCC6/MRP6 mutations: further insight into the molecular pathology of pseudoxanthoma elasticum

J. Wijnholds, A. Plomp, A. Bergen, 2003, European Journal of Human Genetics.

Classification of Dutch and German avian reoviruses by sequencing the sigma C protein.

A. Gielkens, A. ter Huurne, A. Kant, 2003, Veterinary research.

Carrier detection in X‐linked ocular albinism of the Nettleship‐Falls type by DNA analysis

G. Ommen, A. Gal, E. Bleeker-Wagemakers, 1992, Clinical genetics.

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa with preserved para-arteriolar RPE (RP12).

Shomi S. Bhattacharya, F. Cremers, S. Bhattacharya, 2000 .

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

A. Deutman, A. D. den Hollander, H. Brunner, 1999, Nature Genetics.

Genetic variation at the porcine MYF-5 gene locus. Lack of association with meat production traits

W. Buist, M. T. te Pas, F. Harders, 1999, Mammalian Genome.

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.

L. Sandkuijl, A. Bergen, A. Westerveld, 1994, Genomics.

Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosa.

J. Ott, E. Schwinger, L. I. van den Born, 1993, Genomics.

Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family.

P T de Jong, L I van den Born, M J van Schooneveld, 1994, Ophthalmic genetics.