The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.

Por Vollmer, M, Jung, M, Rüschendorf, F, Ruf, R, Wienker, T, Reis, A, Krapf, R, Hildebrandt, F
Publicado em 1998

Genetic dissection of X-linked interspecific hybrid placental dysplasia in congenic mouse strains.

Por Hemberger, M C, Pearsall, R S, Zechner, U, Orth, A, Otto, S, Rüschendorf, F, Fundele, R, Elliott, R
Publicado em 1999

Gene localization for an autosomal dominant familial periodic fever to 12p13.

Por Mulley, J, Saar, K, Hewitt, G, Rüschendorf, F, Phillips, H, Colley, A, Sillence, D, Reis, A, Wilson, M
Publicado em 1998

Molecular karyotyping using an SNP array for genomewide genotyping

Por Rauch, A, Ruschendorf, F, Huang, J, Trautmann, U, Becker, C, Thiel, C, Jones, K, Reis, A, Nurnberg, P
Publicado em 2004

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Por Kaindl, A, Ruschendorf, F, Krause, S, Goebel, H, Koehler, K, Becker, C, Pongratz, D, Muller-Hocker, J, Nurnberg, P, Stoltenburg-Didin..., G, Lochmuller, H, Huebner, A
Publicado em 2004

Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.

Por van Bokhoven, H, Jung, M, Smits, A P, van Beersum, S, Rüschendorf, F, van Steensel, M, Veenstra, M, Tuerlings, J H, Mariman, E C, Brunner, H G, Wienker, T F, Reis, A, Ropers, H H, Hamel, B C
Publicado em 1999