P Nürnberg

发表

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

H. Goebel, H. Lochmüller, F. Rüschendorf, 2004, Journal of Medical Genetics.

A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs

K Konrad, A Dempfle, H Remschmidt, 2006, Molecular Psychiatry.

Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.

D. Seelow, H. Schild, A. Ekici, 2006, American journal of human genetics.

Paternity assessment in rhesus macaques (Macaca mulatta): Multilocus DNA fingerprinting and PCR marker typing

M Krawczak, M Kayser, M. Krawczak, 1998, American journal of primatology.

Molecular karyotyping using an SNP array for genomewide genotyping

F. Rüschendorf, C. Becker, P. Nürnberg, 2004, Journal of Medical Genetics.