Oehlmann R - Search Results

1

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD. Gasser T, et al. Among authors: oehlmann r. Nat Genet. 1998 Mar;18(3):262-5. doi: 10.1038/ng0398-262. Nat Genet. 1998. PMID: 9500549

2

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.

Veske A, Oehlmann R, Younus F, Mohyuddin A, Müller-Myhsok B, Mehdi SQ, Gal A. Veske A, et al. Among authors: oehlmann r. Hum Mol Genet. 1996 Jan;5(1):165-8. doi: 10.1093/hmg/5.1.165. Hum Mol Genet. 1996. PMID: 8789456

3

Genetic complexity and Parkinson's disease.

Gasser T, Müller-Myhsok B, Wszolek ZK, Dürr A, Vaughan JR, Bonifati V, Meco G, Bereznai B, Oehlmann R, Agid Y, Brice A, Wood N. Gasser T, et al. Among authors: oehlmann r. Science. 1997 Jul 18;277(5324):388-9; author reply 389. Science. 1997. PMID: 9518367 No abstract available.

4

Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan.

Leutelt J, Oehlmann R, Younus F, van den Born LI, Weber JL, Denton MJ, Mehdi SQ, Gal A. Leutelt J, et al. Among authors: oehlmann r. Clin Genet. 1995 Mar;47(3):122-4. doi: 10.1111/j.1399-0004.1995.tb03943.x. Clin Genet. 1995. PMID: 7634534

5

Oguchi disease: suggestion of linkage to markers on chromosome 2q.

Maw MA, John S, Jablonka S, Müller B, Kumaramanickavel G, Oehlmann R, Denton MJ, Gal A. Maw MA, et al. Among authors: oehlmann r. J Med Genet. 1995 May;32(5):396-8. doi: 10.1136/jmg.32.5.396. J Med Genet. 1995. PMID: 7616550 Free PMC article.

6

Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19.

Oehlmann R, Summerville GP, Yeh G, Weaver EJ, Jimenez SA, Knowlton RG. Oehlmann R, et al. Am J Hum Genet. 1994 Jan;54(1):3-10. Am J Hum Genet. 1994. PMID: 8279467 Free PMC article.

7

Localization of the Krabbe disease gene (GALC) on chromosome 14 by multipoint linkage analysis.

Oehlmann R, Zlotogora J, Wenger DA, Knowlton RG. Oehlmann R, et al. Am J Hum Genet. 1993 Dec;53(6):1250-5. Am J Hum Genet. 1993. PMID: 8250040 Free PMC article.

8

Missense rhodopsin mutation in a family with recessive RP.

Kumaramanickavel G, Maw M, Denton MJ, John S, Srikumari CR, Orth U, Oehlmann R, Gal A. Kumaramanickavel G, et al. Among authors: oehlmann r. Nat Genet. 1994 Sep;8(1):10-1. doi: 10.1038/ng0994-10. Nat Genet. 1994. PMID: 7987385 No abstract available.

9

Exclusion of type II and type VI procollagen gene mutations in a five-generation family with multiple epiphyseal dysplasia.

Weaver EJ, Summerville GP, Yeh G, Hervada-Page M, Oehlmann R, Rothman R, Jimenez SA, Knowlton RG. Weaver EJ, et al. Among authors: oehlmann r. Am J Med Genet. 1993 Feb 1;45(3):345-52. doi: 10.1002/ajmg.1320450312. Am J Med Genet. 1993. PMID: 8094597

10

Alternatively spliced transcripts of the thymus-specific protease PRSS16 are differentially expressed in human thymus.

Luther C, Wienhold W, Oehlmann R, Heinemann MK, Melms A, Tolosa E. Luther C, et al. Among authors: oehlmann r. Genes Immun. 2005 Feb;6(1):1-7. doi: 10.1038/sj.gene.6364142. Genes Immun. 2005. PMID: 15592422

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