Riess O - Search Results

1

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.

Fang YY, Bain S, Haan EA, Eyre HJ, MacDonald M, Wright TJ, Altherr MR, Riess O, Sutherland G, Callen DF. Fang YY, et al. Among authors: riess o. Am J Med Genet. 1997 Sep 5;71(4):453-7. Am J Med Genet. 1997. PMID: 9286454

2

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

Fang YY, Eyre HJ, Bohlander SK, Estop A, McPherson E, Träger T, Riess O, Callen DF. Fang YY, et al. Among authors: riess o. Am J Hum Genet. 1995 Nov;57(5):1137-42. Am J Hum Genet. 1995. PMID: 7485165 Free PMC article.

3

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).

Wieczorek D, Krause M, Majewski F, Albrecht B, Meinecke P, Riess O, Gillessen-Kaesbach G. Wieczorek D, et al. Among authors: riess o. J Med Genet. 2000 Oct;37(10):798-804. doi: 10.1136/jmg.37.10.798. J Med Genet. 2000. PMID: 11183188 Free PMC article. No abstract available.

4

Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.

Wieczorek D, Krause M, Majewski F, Albrecht B, Horn D, Riess O, Gillessen-Kaesbach G. Wieczorek D, et al. Among authors: riess o. Eur J Hum Genet. 2000 Jul;8(7):519-26. doi: 10.1038/sj.ejhg.5200498. Eur J Hum Genet. 2000. PMID: 10909852

5

Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region.

Weber B, Hedrick A, Andrew S, Riess O, Collins C, Kowbel D, Hayden MR. Weber B, et al. Among authors: riess o. Am J Hum Genet. 1992 Feb;50(2):382-93. Am J Hum Genet. 1992. PMID: 1346482 Free PMC article.

6

Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease.

Weber B, Riess O, Wolff G, Andrew S, Collins C, Graham R, Theilmann J, Hayden MR. Weber B, et al. Among authors: riess o. Nat Genet. 1992 Nov;2(3):216-22. doi: 10.1038/ng1192-216. Nat Genet. 1992. PMID: 1345172

7

(CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16.

Riess O, Weber B, Hayden MR. Riess O, et al. Hum Mol Genet. 1992 Sep;1(6):452. doi: 10.1093/hmg/1.6.452. Hum Mol Genet. 1992. PMID: 1338762 No abstract available.

8

(CA)n-dinucleotide repeat at the PDEB locus in 4p16.3.

Weber B, Riess O, Daneshvar H, Graham R, Hayden MR. Weber B, et al. Among authors: riess o. Hum Mol Genet. 1993 Jun;2(6):827. doi: 10.1093/hmg/2.6.827. Hum Mol Genet. 1993. PMID: 8394765 No abstract available.

9

cDNA cloning and expression of rsca1, the rat counterpart of the human spinocerebellar ataxia type 1 gene.

Gossen M, Schmitt I, Obst K, Wahle P, Epplen JT, Riess O. Gossen M, et al. Among authors: riess o. Hum Mol Genet. 1996 Mar;5(3):381-9. doi: 10.1093/hmg/5.3.381. Hum Mol Genet. 1996. PMID: 8852664

10

A polymorphic DNA marker at the D8S131 locus.

Weber B, Riess O, Kreklywich CN, Wood S, Hayden MR. Weber B, et al. Among authors: riess o. Nucleic Acids Res. 1991 Apr 11;19(7):1725. Nucleic Acids Res. 1991. PMID: 1674144 Free PMC article.

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