Reis A - Search Results

1

Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree.

Omran H, Fernandez C, Jung M, Häffner K, Fargier B, Villaquiran A, Waldherr R, Gretz N, Brandis M, Rüschendorf F, Reis A, Hildebrandt F. Omran H, et al. Among authors: reis a. Am J Hum Genet. 2000 Jan;66(1):118-27. doi: 10.1086/302705. Am J Hum Genet. 2000. PMID: 10631142 Free PMC article.

2

Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12-q21.

Reis A, Küster W, Eckardt R, Sperling K. Reis A, et al. Hum Genet. 1992 Sep-Oct;90(1-2):113-6. doi: 10.1007/BF00210752. Hum Genet. 1992. PMID: 1385292

3

Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplification.

Spielvogel H, Hennies HC, Claussen U, Washington SS, Chakravarti A, Reis A. Spielvogel H, et al. Among authors: reis a. Am J Hum Genet. 1992 May;50(5):1031-7. Am J Hum Genet. 1992. PMID: 1570832 Free PMC article.

4

Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster.

Hennies HC, Küster W, Mischke D, Reis A. Hennies HC, et al. Among authors: reis a. Hum Mol Genet. 1995 Jun;4(6):1015-20. doi: 10.1093/hmg/4.6.1015. Hum Mol Genet. 1995. PMID: 7544663

5

Recurrent nasal polyps as a monosymptomatic form of cystic fibrosis associated with a novel in-frame deletion (591del18) in the CFTR gene.

Varon R, Magdorf K, Staab D, Wahn HU, Krawczak M, Sperling K, Reis A. Varon R, et al. Among authors: reis a. Hum Mol Genet. 1995 Aug;4(8):1463-4. doi: 10.1093/hmg/4.8.1463. Hum Mol Genet. 1995. PMID: 7581390 No abstract available.

6

Trinucleotide repeat polymorphism at the PKLR locus.

Lenzner C, Jacobasch G, Reis A, Thiele B, Nürnberg P. Lenzner C, et al. Among authors: reis a. Hum Mol Genet. 1994 Mar;3(3):523. doi: 10.1093/hmg/3.3.523-a. Hum Mol Genet. 1994. PMID: 8012373 No abstract available.

7

Linkage analysis in German breast cancer families with early onset of the disease, using highly polymorphic markers from the chromosome 17q11-q24 region.

Zimmermann W, Bender E, Rohde K, Reis A, Wiseman R, Futreal A, Krause H, Prokoph H, Werner S, Scherneck S. Zimmermann W, et al. Among authors: reis a. Am J Hum Genet. 1993 Apr;52(4):789-91. Am J Hum Genet. 1993. PMID: 8460645 Free PMC article.

8

Three dinucleotide microsatellite polymorphisms on human chromosome 13.

Hennies HC, Reis A. Hennies HC, et al. Among authors: reis a. Hum Mol Genet. 1993 Jan;2(1):87. doi: 10.1093/hmg/2.1.87. Hum Mol Genet. 1993. PMID: 8490630 No abstract available.

9

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.

Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A. Bürger J, et al. Among authors: reis a. Hum Genet. 1996 Sep;98(3):371-5. doi: 10.1007/s004390050223. Hum Genet. 1996. PMID: 8707310

10

Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster.

Weber A, Wienker TF, Jung M, Easton D, Dean HJ, Heinrichs C, Reis A, Clark AJ. Weber A, et al. Among authors: reis a. Hum Mol Genet. 1996 Dec;5(12):2061-6. doi: 10.1093/hmg/5.12.2061. Hum Mol Genet. 1996. PMID: 8968764

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3,433 results

Search Page

Filters