Köhler A - Search Results

1

Assignment of genes encoding GABAA receptor subunits alpha 1, alpha 6, beta 2, and gamma 2 to a YAC contig of 5q33.

Kostrzewa M, Köhler A, Eppelt K, Hellam L, Fairweather ND, Levy ER, Monaco AP, Müller U. Kostrzewa M, et al. Among authors: kohler a. Eur J Hum Genet. 1996;4(4):199-204. doi: 10.1159/000472199. Eur J Hum Genet. 1996. PMID: 8875185

2

Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1.

Haberhausen G, Schmitt I, Köhler A, Peters U, Rider S, Chelly J, Terwilliger JD, Monaco AP, Müller U. Haberhausen G, et al. Among authors: kohler a. Am J Hum Genet. 1995 Sep;57(3):644-50. Am J Hum Genet. 1995. PMID: 7668293 Free PMC article.

3

Integrated physical and transcript map of 5q31.3-qter.

Kostrzewa M, Krings BW, Dixon MJ, Eppelt K, Köhler A, Grady DL, Steinberger D, Fairweather ND, Moyzis RK, Monaco AP, Müller U. Kostrzewa M, et al. Among authors: kohler a. Eur J Hum Genet. 1998 May-Jun;6(3):266-74. doi: 10.1038/sj.ejhg.5200188. Eur J Hum Genet. 1998. PMID: 9781031

4

Clinical and molecular genetic findings in five patients with Miller-Dieker syndrome.

Köhler A, Hain J, Müller U. Köhler A, et al. Clin Genet. 1995 Mar;47(3):161-4. doi: 10.1111/j.1399-0004.1995.tb03951.x. Clin Genet. 1995. PMID: 7634541

5

Familial half cryptic translocation t(9;17).

Köhler A, Hain J, Müller U. Köhler A, et al. J Med Genet. 1994 Sep;31(9):712-4. doi: 10.1136/jmg.31.9.712. J Med Genet. 1994. PMID: 7815441 Free PMC article.

6

Molecular basis and diagnosis of neurogenetic disorders.

Müller U, Graeber MB, Haberhausen G, Köhler A. Müller U, et al. Among authors: kohler a. J Neurol Sci. 1994 Jul;124(2):119-40. doi: 10.1016/0022-510x(94)90318-2. J Neurol Sci. 1994. PMID: 7964863 Review.

7

Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndrome.

Weber A, Köhler A, Hahn A, Neubauer B, Müller U. Weber A, et al. Among authors: kohler a. Neurogenetics. 2013 Nov;14(3-4):251-3. doi: 10.1007/s10048-013-0376-7. Epub 2013 Oct 8. Neurogenetics. 2013. PMID: 24100940

8

8p23.1 duplication syndrome: narrowing of critical interval to 1.80 Mbp.

Weber A, Köhler A, Hahn A, Müller U. Weber A, et al. Among authors: kohler a. Mol Cytogenet. 2014 Dec 9;7(1):94. doi: 10.1186/s13039-014-0094-3. eCollection 2014. Mol Cytogenet. 2014. PMID: 25520754 Free PMC article.

9

DYT7 gene locus for cervical dystonia on chromosome 18p is questionable.

Winter P, Kamm C, Biskup S, Köhler A, Leube B, Auburger G, Gasser T, Benecke R, Müller U. Winter P, et al. Among authors: kohler a. Mov Disord. 2012 Dec;27(14):1819-21. doi: 10.1002/mds.25219. Epub 2012 Oct 31. Mov Disord. 2012. PMID: 23115116

10

Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt.

Kohlhase J, Schuh R, Dowe G, Kühnlein RP, Jäckle H, Schroeder B, Schulz-Schaeffer W, Kretzschmar HA, Köhler A, Müller U, Raab-Vetter M, Burkhardt E, Engel W, Stick R. Kohlhase J, et al. Among authors: kohler a. Genomics. 1996 Dec 15;38(3):291-8. doi: 10.1006/geno.1996.0631. Genomics. 1996. PMID: 8975705

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