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American Journal of Respiratory Cell and Molecular Biology|November 4, 2000
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate geneH Omran, K Häffner, A Völkel, et al.
Nature Genetics|April 1, 1993
A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2pC Antignac, C H Arduy, J S Beckmann, et al.
Biochimica Et Biophysica Acta|December 2, 1991
Cloning, sequence, and tissue distribution of a rabbit renal Na+/H+ exchanger transcriptF Hildebrandt, J H Pizzonia, R F Reilly, et al.
American Journal of Human Genetics|January 23, 1999
Hereditary isolated renal magnesium loss maps to chromosome 11q23I C Meij, K Saar, L P van den Heuvel, et al.
Pediatric Nephrology (Berlin, Germany)|March 21, 1998
Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische NephrologieF Hildebrandt, H G Nothwang, U Vossmerbäumer, et al.
American Journal of Human Genetics|January 13, 2000
Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigreeH Omran, C Fernandez, M Jung, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 27, 1998
Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneityA Fuchshuber, C C Deltas, S Berthold, et al.
Genomics|June 13, 2001
Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the regionA Fuchshuber, S Kroiss, S Karle, et al.
Genomics|May 1, 1997
Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13H G Nothwang, B Strahm, D Denich, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophyA M Lehman, P Eydoux, D Doherty, et al.
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