Reis A - Search Results

1

Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).

Reis A, Hennies HC, Langbein L, Digweed M, Mischke D, Drechsler M, Schröck E, Royer-Pokora B, Franke WW, Sperling K, et al. Reis A, et al. Nat Genet. 1994 Feb;6(2):174-9. doi: 10.1038/ng0294-174. Nat Genet. 1994. PMID: 7512862

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

[Vörner keratosis palmoplantaris diffusa. Clinical, formal genetic and molecular biology studies of 22 families].

Küster W, Zehender D, Mensing H, Hennies HC, Reis A. Küster W, et al. Among authors: reis a. Hautarzt. 1995 Oct;46(10):705-10. doi: 10.1007/s001050050326. Hautarzt. 1995. PMID: 7499131 German.

5

Keratin 9 gene mutational heterogeneity in patients with epidermolytic palmoplantar keratoderma.

Hennies HC, Zehender D, Kunze J, Küster W, Reis A. Hennies HC, et al. Among authors: reis a. Hum Genet. 1994 Jun;93(6):649-54. doi: 10.1007/BF00201564. Hum Genet. 1994. PMID: 7516304

6

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

7

The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1.

Stumm M, Gatti RA, Reis A, Udar N, Chrzanowska K, Seemanova E, Sperling K, Wegner RD. Stumm M, et al. Among authors: reis a. Am J Hum Genet. 1995 Oct;57(4):960-2. Am J Hum Genet. 1995. PMID: 7573059 Free PMC article. No abstract available.

8

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.

9

Environmental trichlorfon and cluster of congenital abnormalities.

Czeizel AE, Elek C, Gundy S, Métneki J, Nemes E, Reis A, Sperling K, Tímár L, Tusnády G, Virágh Z. Czeizel AE, et al. Among authors: reis a. Lancet. 1993 Feb 27;341(8844):539-42. doi: 10.1016/0140-6736(93)90293-p. Lancet. 1993. PMID: 8094783

10

Dinucleotide repeat polymorphism at the locus D13S231.

Saksová L, Hennies HC, Reis A. Saksová L, et al. Among authors: reis a. Hum Mol Genet. 1993 Jul;2(7):1082. doi: 10.1093/hmg/2.7.1082-a. Hum Mol Genet. 1993. PMID: 8364558 No abstract available.

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