Liehr T - Search Results

1

PDE3A mutations cause autosomal dominant hypertension with brachydactyly.

Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein E, Mühl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, Ott J, Rittscher K, Liehr T, Jordan J, Plessis G, Tank J, Mai K, Naraghi R, Hodge R, Hopp M, Hattenbach LO, Busjahn A, Rauch A, Vandeput F, Gong M, Rüschendorf F, Hübner N, Haller H, Mundlos S, Bilginturan N, Movsesian MA, Klussmann E, Toka O, Bähring S. Maass PG, et al. Among authors: liehr t. Nat Genet. 2015 Jun;47(6):647-53. doi: 10.1038/ng.3302. Epub 2015 May 11. Nat Genet. 2015. PMID: 25961942 Free article.

2

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH).

Rauch A, Pfeiffer RA, Trautmann U, Liehr T, Rott HD, Ulmer R. Rauch A, et al. Among authors: liehr t. Clin Genet. 1992 Aug;42(2):84-90. doi: 10.1111/j.1399-0004.1992.tb03145.x. Clin Genet. 1992. PMID: 1424236

3

Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion.

Liehr T, Rautenstrauss B, Grehl H, Bathke KD, Ekici A, Rauch A, Rott HD. Liehr T, et al. Hum Genet. 1996 Jul;98(1):22-8. doi: 10.1007/s004390050154. Hum Genet. 1996. PMID: 8682501

4

Evidence for interphase DNA decondensation transverse to the chromosome axis: a multicolor banding analysis.

Weise A, Starke H, Heller A, Uwe C, Liehr T. Weise A, et al. Among authors: liehr t. Int J Mol Med. 2002 Apr;9(4):359-61. Int J Mol Med. 2002. PMID: 11891527

5

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes.

Weise A, Starke H, Heller A, Tönnies H, Volleth M, Stumm M, Gabriele S, Nietzel A, Claussen U, Liehr T. Weise A, et al. Among authors: liehr t. J Med Genet. 2002 Jun;39(6):434-9. doi: 10.1136/jmg.39.6.434. J Med Genet. 2002. PMID: 12070255 Free PMC article. No abstract available.

6

Fluorescence in situ hybridization (FISH) on human chromosomes using photoprobe biotin-labeled probes.

Weise A, Harbarth P, Claussen U, Liehr T. Weise A, et al. Among authors: liehr t. J Histochem Cytochem. 2003 Apr;51(4):549-51. doi: 10.1177/002215540305100418. J Histochem Cytochem. 2003. PMID: 12642635

7

Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines.

Weise A, Liehr T, Efferth T, Kuechler A, Gebhart E. Weise A, et al. Among authors: liehr t. Cytogenet Genome Res. 2002;98(2-3):118-25. doi: 10.1159/000069808. Cytogenet Genome Res. 2002. PMID: 12697993

8

Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10].

Sauter S, von Beust G, Burfeind P, Weise A, Starke H, Liehr T, Zoll B. Sauter S, et al. Among authors: liehr t. Am J Med Genet A. 2003 Aug 1;120A(4):533-6. doi: 10.1002/ajmg.a.20089. Am J Med Genet A. 2003. PMID: 12884434

9

Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.

Polityko A, Maltseva O, Rumyantseva N, Khurs O, Seidel J, Claussen U, Weise A, Liehr T, Starke H. Polityko A, et al. Among authors: liehr t. Int J Mol Med. 2004 Dec;14(6):977-9. Int J Mol Med. 2004. PMID: 15547662

10

Evolution versus constitution: differences in chromosomal inversion.

Schmidt S, Claussen U, Liehr T, Weise A. Schmidt S, et al. Among authors: liehr t. Hum Genet. 2005 Jul;117(2-3):213-9. doi: 10.1007/s00439-005-1294-z. Epub 2005 May 11. Hum Genet. 2005. PMID: 15886998

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