Eggermann T - Search Results

1

Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals.

Markov V, Krug A, Krach S, Whitney C, Eggermann T, Zerres K, Stöcker T, Shah NJ, Nöthen MM, Treutlein J, Rietschel M, Kircher T. Markov V, et al. Among authors: eggermann t. Neuroimage. 2009 Oct 1;47(4):2016-22. doi: 10.1016/j.neuroimage.2009.05.067. Epub 2009 Jun 1. Neuroimage. 2009. PMID: 19497374

2

Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling.

Eggermann T, Nöthen MM, Propping P, Schwanitz G. Eggermann T, et al. Ann Genet. 1993;36(4):214-6. Ann Genet. 1993. PMID: 8166427

3

Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome).

Nöthen MM, Eggermann T, Erdmann J, Eiben B, Hofmann D, Propping P, Schwanitz G. Nöthen MM, et al. Among authors: eggermann t. Hum Genet. 1993 Oct;92(4):347-9. doi: 10.1007/BF01247332. Hum Genet. 1993. PMID: 8225314

4

Origin of uniparental disomy 6: presentation of a new case and review on the literature.

Eggermann T, Marg W, Mergenthaler S, Eggermann K, Schemmel V, Stoffers U, Zerres K, Spranger S. Eggermann T, et al. Among authors: eggermann k. Ann Genet. 2001 Jan-Mar;44(1):41-5. doi: 10.1016/s0003-3995(01)01035-8. Ann Genet. 2001. PMID: 11334617 Review.

5

DNA diagnosis in hereditary nephropathies.

Zerres K, Eggermann T, Rudnik-Schöneborn S. Zerres K, et al. Among authors: eggermann t. Clin Nephrol. 2001 Sep;56(3):181-92. Clin Nephrol. 2001. PMID: 11597032

6

[Molecular biology of cystinuria].

Albers A, Wagner CA, Schmidt C, Lahme S, Bichler KH, Lang F, Zerres K, Eggermann T. Albers A, et al. Among authors: eggermann t. Fortschr Med Orig. 2001;119(1):49-50. Fortschr Med Orig. 2001. PMID: 11935659 German.

7

Uniparental disomy: clinical indications for testing in growth retardation.

Eggermann T, Zerres K, Eggermann K, Moore G, Wollmann HA. Eggermann T, et al. Among authors: eggermann k. Eur J Pediatr. 2002 Jun;161(6):305-12. doi: 10.1007/s00431-002-0916-x. Epub 2002 Apr 26. Eur J Pediatr. 2002. PMID: 12029448 Review.

8

Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the disease.

Schmidt C, Albers A, Tomiuk J, Eggermann K, Wagner C, Capasso G, Lahme S, Hesse A, Lang F, Zerres K, Eggermann T. Schmidt C, et al. Among authors: eggermann k, eggermann t. Clin Nephrol. 2002 May;57(5):342-8. doi: 10.5414/cnp57342. Clin Nephrol. 2002. PMID: 12036192

9

Phenotype diversity in familial cylindromatosis: a frameshift mutation in the tumor suppressor gene CYLD underlies different tumors of skin appendages.

Poblete Gutiérrez P, Eggermann T, Höller D, Jugert FK, Beermann T, Grussendorf-Conen EI, Zerres K, Merk HF, Frank J. Poblete Gutiérrez P, et al. Among authors: eggermann t. J Invest Dermatol. 2002 Aug;119(2):527-31. doi: 10.1046/j.1523-1747.2002.01839.x. J Invest Dermatol. 2002. PMID: 12190880 Free article.

10

Allelic variants in the 5' non-coding region of the connexin32 gene: possible pitfalls in the diagnosis of X linked Charcot-Marie-Tooth neuropathy (CMTX).

Bergmann C, Zerres K, Rudnik-Schöneborn S, Eggermann T, Schröder JM, Senderek J. Bergmann C, et al. Among authors: eggermann t. J Med Genet. 2002 Sep;39(9):e58. doi: 10.1136/jmg.39.9.e58. J Med Genet. 2002. PMID: 12205128 Free PMC article. No abstract available.

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