Friedhelm Hildebrandt

Construction of a gene map of the nephronophthisis type 1 (NPHP1) region on human chromosome 2q12-q13.

P. Lichter, F. Hildebrandt, H. Nothwang, 1998, Genomics.

Refined genetic mapping of a gene for familial juvenile nephronophthisis (NPH1) and physical mapping of linked markers. APN Study Group.

F. Hildebrandt, T. Papenfuss, M. Brandis, 1995, Genomics.

Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.

C. Antignac, F. Hildebrandt, L. Guay-Woodford, 2000, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Hereditary isolated renal magnesium loss maps to chromosome 11q23.

F. Hildebrandt, L. P. Van den Heuvel, A. Reis, 1999, American journal of human genetics.