Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

מאת Eiberg, H, Hansen, L, Kjer, B, Hansen, T, Pedersen, O, Bille, M, Rosenberg, T, Tranebjærg, L
יצא לאור 2006

Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)

מאת Kjaer, K, Hansen, L, Schwabe, G, Marques-de-Faria, A, Eiberg, H, Mundlos, S, Tommerup, N, Rosenberg, T
יצא לאור 2005

A mutation in the receptor binding site of GDF5 causes Mohr‐Wriedt brachydactyly type A2

מאת Kjaer, K W, Eiberg, H, Hansen, L, van der Hagen, C B, Rosendahl, K, Tommerup, N, Mundlos, S
יצא לאור 2006

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study

מאת Nielsen, J, Krabbe, K, Jennum, P, Koefoed, P, Jensen, L, Fenger, K, Eiberg, H, Hasholt, L, Werdelin, L, Sorensen, S
יצא לאור 1998

Loss of heterozygosity at 9q33 and hypermethylation of the DBCCR1 gene in oral squamous cell carcinoma

מאת Gao, S, Worm, J, Guldberg, P, Eiberg, H, Krogdahl, A, Sørensen, J A, Liu, C-J, Reibel, J, Dabelsteen, E
יצא לאור 2004

An exclusion map of Marfan syndrome.

מאת Blanton, S H, Sarfarazi, M, Eiberg, H, de Groote, J, Farndon, P A, Kilpatrick, M W, Child, A H, Pope, F M, Peltonen, L, Francomano, C A
יצא לאור 1990

Linkage studies of Friedreich ataxia by means of blood-group and protein markers

מאת Keats, B. J. B., Ward, L. J., Lu, M., Krieger, S., Wilensky, M. A., Forster-Gibson, C. J., Roy, M., Monté, M., Barbeau, A., Simpson, N. E., Eiberg, H., Tippett, P., Williamson, R., Chamberlain, S.
יצא לאור 1987