Liehr T - Search Results

1

Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16.

Balikova I, Martens K, Melotte C, Amyere M, Van Vooren S, Moreau Y, Vetrie D, Fiegler H, Carter NP, Liehr T, Vikkula M, Matthijs G, Fryns JP, Casteels I, Devriendt K, Vermeesch JR. Balikova I, et al. Among authors: liehr t. Am J Hum Genet. 2008 Jan;82(1):181-7. doi: 10.1016/j.ajhg.2007.08.001. Am J Hum Genet. 2008. PMID: 18179897 Free PMC article.

2

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

3

Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3-q25.2 and mutation analysis.

Michels-Rautenstrauss KG, Mardin CY, Budde WM, Liehr T, Polansky J, Nguyen T, Timmerman V, Van Broeckhoven C, Naumann GO, Pfeiffer RA, Rautenstrauss BW. Michels-Rautenstrauss KG, et al. Among authors: liehr t. Hum Genet. 1998 Jan;102(1):103-6. doi: 10.1007/s004390050661. Hum Genet. 1998. PMID: 9490287

4

Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminoma.

von Deimling F, Scharf JM, Liehr T, Rothe M, Kelter AR, Albers P, Dietrich WF, Kunkel LM, Wernert N, Wirth B. von Deimling F, et al. Among authors: liehr t. Hum Genet. 1999 Jul-Aug;105(1-2):17-27. doi: 10.1007/s004399900067. Hum Genet. 1999. PMID: 10480350

5

The DNA-based structure of human chromosome 5 in interphase.

Lemke J, Claussen J, Michel S, Chudoba I, Mühlig P, Westermann M, Sperling K, Rubtsov N, Grummt UW, Ullmann P, Kromeyer-Hauschild K, Liehr T, Claussen U. Lemke J, et al. Among authors: liehr t. Am J Hum Genet. 2002 Nov;71(5):1051-9. doi: 10.1086/344286. Epub 2002 Oct 7. Am J Hum Genet. 2002. PMID: 12370837 Free PMC article.

6

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

7

Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.

von Beust G, Sauter SM, Liehr T, Burfeind P, Bartels I, Starke H, von Eggeling F, Zoll B. von Beust G, et al. Among authors: liehr t. Am J Med Genet A. 2005 Aug 15;137(1):59-64. doi: 10.1002/ajmg.a.30835. Am J Med Genet A. 2005. PMID: 16007665 Review.

8

Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.

Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns JP, Liehr T. Vermeesch JR, et al. Among authors: liehr t. Eur J Med Genet. 2005 Jul-Sep;48(3):319-27. doi: 10.1016/j.ejmg.2005.04.018. Eur J Med Genet. 2005. PMID: 16179227

9

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.

Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR. Liehr T, et al. Am J Med Genet A. 2006 Jan 1;140(1):46-51. doi: 10.1002/ajmg.a.31048. Am J Med Genet A. 2006. PMID: 16333826 Review.

10

Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies.

Balci S, Engiz O, Aktaş D, Vargel I, Beksaç MS, Mrasek K, Vermeesch J, Liehr T. Balci S, et al. Among authors: liehr t. Am J Med Genet A. 2006 Mar 15;140(6):628-32. doi: 10.1002/ajmg.a.31131. Am J Med Genet A. 2006. PMID: 16470698

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