Hildebrandt F - Search Results

1

Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease.

Kroiss S, Huck K, Berthold S, Rüschendorf F, Scolari F, Caridi G, Ghiggeri GM, Hildebrandt F, Fuchshuber A. Kroiss S, et al. Among authors: hildebrandt f. Nephrol Dial Transplant. 2000 Jun;15(6):818-21. doi: 10.1093/ndt/15.6.818. Nephrol Dial Transplant. 2000. PMID: 10831633

2

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

Hildebrandt F, Singh-Sawhney I, Schnieders B, Papenfuss T, Brandis M. Hildebrandt F, et al. Genomics. 1995 Jan 20;25(2):360-4. doi: 10.1016/0888-7543(95)80034-j. Genomics. 1995. PMID: 7789968

3

LODVIEW: a computer program for the graphical evaluation of lod score results in exclusion mapping of human disease genes.

Hildebrandt F, Pohlmann A, Omran H. Hildebrandt F, et al. Comput Biomed Res. 1993 Dec;26(6):592-9. doi: 10.1006/cbmr.1993.1042. Comput Biomed Res. 1993. PMID: 8112059

4

Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study Group.

Hildebrandt F, Singh-Sawhney I, Schnieders B, Centofante L, Omran H, Pohlmann A, Schmaltz C, Wedekind H, Schubotz C, Antignac C, et al. Hildebrandt F, et al. Am J Hum Genet. 1993 Dec;53(6):1256-61. Am J Hum Genet. 1993. PMID: 8250041 Free PMC article.

5

Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13.

Hildebrandt F, Cybulla M, Strahm B, Nothwang HG, Singh-Sawhney I, Berz K, Nicklin M, Reiner O, Brandis M. Hildebrandt F, et al. Cytogenet Cell Genet. 1996;73(3):235-9. doi: 10.1159/000134346. Cytogenet Cell Genet. 1996. PMID: 8697815

6

Glomerulopathy associated with predominant fibronectin deposits: exclusion of the genes for fibronectin, villin and desmin as causative genes.

Hildebrandt F, Strahm B, Prochoroff A, Cybulla M, Gemperle O, Krapf R, Brandis M. Hildebrandt F, et al. Am J Med Genet. 1996 May 3;63(1):323-7. doi: 10.1002/(SICI)1096-8628(19960503)63:1<323::AID-AJMG54>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8723129

7

Late occurrence of cysts in autosomal dominant medullary cystic kidney disease.

Neumann HP, Zäuner I, Strahm B, Bender BU, Schollmeyer P, Blum U, Rohrbach R, Hildebrandt F. Neumann HP, et al. Among authors: hildebrandt f. Nephrol Dial Transplant. 1997 Jun;12(6):1242-6. doi: 10.1093/ndt/12.6.1242. Nephrol Dial Transplant. 1997. PMID: 9198059

8

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

Nothwang HG, Stubanus M, Adolphs J, Hanusch H, Vossmerbäumer U, Denich D, Kübler M, Mincheva A, Lichter P, Hildebrandt F. Nothwang HG, et al. Among authors: hildebrandt f. Genomics. 1998 Jan 15;47(2):276-85. doi: 10.1006/geno.1997.5102. Genomics. 1998. PMID: 9479500

9

Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie.

Hildebrandt F, Nothwang HG, Vossmerbäumer U, Springer C, Strahm B, Hoppe B, Keuth B, Fuchshuber A, Querfeld U, Neuhaus TJ, Brandis M. Hildebrandt F, et al. Pediatr Nephrol. 1998 Jan;12(1):16-9. doi: 10.1007/s004670050394. Pediatr Nephrol. 1998. PMID: 9502560

10

Linkage and allelic association of atopy and markers flanking the IL4-receptor gene.

Deichmann KA, Heinzmann A, Forster J, Dischinger S, Mehl C, Brueggenolte E, Hildebrandt F, Moseler M, Kuehr J. Deichmann KA, et al. Among authors: hildebrandt f. Clin Exp Allergy. 1998 Feb;28(2):151-5. doi: 10.1046/j.1365-2222.1998.00159.x. Clin Exp Allergy. 1998. PMID: 9515586

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