Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26

Por Bayoumi, R., Saar, K., Lee, Y., Nurnberg, G., Reis, A., Nur-E-Kamal, M., Al-Gazali, L.
Publicado em 2001

A Novel Familial BBS12 Mutation Associated with a Mild Phenotype: Implications for Clinical and Molecular Diagnostic Strategies

Por Pawlik, B., Mir, A., Iqbal, H., Li, Y., Nürnberg, G., Becker, C., Qamar, R., Nürnberg, P., Wollnik, B.
Publicado em 2010

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.

Por Saar, K, Chrzanowska, K H, Stumm, M, Jung, M, Nürnberg, G, Wienker, T F, Seemanová, E, Wegner, R D, Reis, A, Sperling, K
Publicado em 1997

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

Por Ruf, R, Berkman, J, Wolf, M, Nurnberg, P, Gattas, M, Ruf, E, Hyland, V, Kromberg, J, Glass, I, Macmillan, J, Otto, E, Nurnberg, G, Lucke, B, Hennies, H, Hildebrandt, F
Publicado em 2003

Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia

Por Bergmann, C. , Senderek, J. , Anhuf, D. , Thiel, C. T. , Ekici, A. B. , Poblete-Gutiérrez, P. , van Steensel, M. , Seelow, D. , Nürnberg, G. , Schild, H. H. , Nürnberg, P. , Reis, A. , Frank, J. , Zerres, K. 
Publicado em 2006