Martijn H. Breuning

Location of mutations within the PKD2 gene influences clinical outcome.

D Ravine, M Krawczak, M. Krawczak, 2000, Kidney international.

RT-PCR diagnosis of patients with acute nonlymphocytic leukemia and inv(16)(p13q22) and identification of new alternative splicing in CBFB-MYH11 transcripts.

A. Hagemeijer, B. V. D. Reijden, R. Giles, 1995, Blood.

Myocardial Infarction in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)

P. Macfarlane, M. Ferrari, H. V. van Houwelingen, 2003, Medicine.

Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.

W. Reardon, K. Devriendt, O. Gabrielli, 1999, American journal of human genetics.

Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease.

S. Scherer, P. Taschner, A. Odermatt, 1997, Genomics.