Reis A - Search Results

1

Genome sequencing in families with congenital limb malformations.

Elsner J, Mensah MA, Holtgrewe M, Hertzberg J, Bigoni S, Busche A, Coutelier M, de Silva DC, Elçioglu N, Filges I, Gerkes E, Girisha KM, Graul-Neumann L, Jamsheer A, Krawitz P, Kurth I, Markus S, Megarbane A, Reis A, Reuter MS, Svoboda D, Teller C, Tuysuz B, Türkmen S, Wilson M, Woitschach R, Vater I, Caliebe A, Hülsemann W, Horn D, Mundlos S, Spielmann M. Elsner J, et al. Among authors: reis a. Hum Genet. 2021 Aug;140(8):1229-1239. doi: 10.1007/s00439-021-02295-y. Epub 2021 Jun 22. Hum Genet. 2021. PMID: 34159400 Free PMC article.

2

Cloning and sequence analysis of the human parathyroid hormone gene region.

Reis A, Hecht W, Gröger R, Böhm I, Cooper DN, Lindenmaier W, Mayer H, Schmidtke J. Reis A, et al. Hum Genet. 1990 Jan;84(2):119-24. doi: 10.1007/BF00208924. Hum Genet. 1990. PMID: 2298446

3

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

4

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.

5

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

Reis A, Dittrich B, Greger V, Buiting K, Lalande M, Gillessen-Kaesbach G, Anvret M, Horsthemke B. Reis A, et al. Am J Hum Genet. 1994 May;54(5):741-7. Am J Hum Genet. 1994. PMID: 8178815 Free PMC article.

6

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.

7

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.

8

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

9

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

10

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.

Saar K, Chrzanowska KH, Stumm M, Jung M, Nürnberg G, Wienker TF, Seemanová E, Wegner RD, Reis A, Sperling K. Saar K, et al. Among authors: reis a. Am J Hum Genet. 1997 Mar;60(3):605-10. Am J Hum Genet. 1997. PMID: 9042920 Free PMC article.

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