Froster UG - Search Results

1

New mutations of EXT1 and EXT2 genes in German patients with Multiple Osteochondromas.

Heinritz W, Hüffmeier U, Strenge S, Miterski B, Zweier C, Leinung S, Bohring A, Mitulla B, Peters U, Froster UG. Heinritz W, et al. Among authors: froster ug. Ann Hum Genet. 2009 May;73(Pt 3):283-91. doi: 10.1111/j.1469-1809.2009.00508.x. Epub 2009 Mar 25. Ann Hum Genet. 2009. PMID: 19344451

2

The human TBX5 gene mutation database.

Heinritz W, Shou L, Moschik A, Froster UG. Heinritz W, et al. Among authors: froster ug. Hum Mutat. 2005 Oct;26(4):397. doi: 10.1002/humu.9375. Hum Mutat. 2005. PMID: 16134140

3

A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype.

Heinritz W, Zweier C, Froster UG, Strenge S, Kujat A, Syrbe S, Rauch A, Schuster V. Heinritz W, et al. Among authors: froster ug. Am J Med Genet A. 2006 Jun 1;140(11):1223-7. doi: 10.1002/ajmg.a.31267. Am J Med Genet A. 2006. PMID: 16688751

4

Different phenotypes including gynecological cancer in three female patients with Peutz-Jeghers syndrome and mutations in the STK11 gene.

Heinritz W, Strenge S, Kujat A, Hockel M, Froster UG. Heinritz W, et al. Among authors: froster ug. Onkologie. 2008 Nov;31(11):625-8. doi: 10.1159/000162284. Epub 2008 Oct 27. Onkologie. 2008. PMID: 19145097

5

Microcephaly-lymphedema syndrome: report of a family with short stature as additional manifestation.

Strenge S, Froster UG. Strenge S, et al. Among authors: froster ug. Am J Med Genet. 1998 Dec 28;80(5):506-9. doi: 10.1002/(sici)1096-8628(19981228)80:5<506::aid-ajmg13>3.0.co;2-1. Am J Med Genet. 1998. PMID: 9880217

6

[Hereditary multiple exostoses. Molecular genetic analysis of the EXT1 gene in an unusual family].

Heinritz W, Pretzsch M, Koall S, Matzen PF, Froster UG. Heinritz W, et al. Among authors: froster ug. Orthopade. 2005 May;34(5):470-6. doi: 10.1007/s00132-005-0774-0. Orthopade. 2005. PMID: 15739063 German.

7

Evidence for a founder effect of the germline fumarate hydratase gene mutation R58P causing hereditary leiomyomatosis and renal cell cancer (HLRCC).

Heinritz W, Paasch U, Sticherling M, Wittekind C, Simon JC, Froster UG, Renner R. Heinritz W, et al. Among authors: froster ug. Ann Hum Genet. 2008 Jan;72(Pt 1):35-40. doi: 10.1111/j.1469-1809.2007.00396.x. Epub 2006 Oct 1. Ann Hum Genet. 2008. PMID: 17908262

8

[Molecular genetic mutation analysis of the PTPN11 gene in the multiple lentigines (LEOPARD) syndrome].

Froster UG, Glander HJ, Heinritz W. Froster UG, et al. Hautarzt. 2003 Dec;54(12):1190-2. doi: 10.1007/s00105-003-0640-0. Hautarzt. 2003. PMID: 14634749 German.

9

Macular corneal dystrophy: mutational spectrum in German patients, novel mutations and therapeutic options.

Gruenauer-Kloevekorn C, Braeutigam S, Heinritz W, Froster UG, Duncker GI. Gruenauer-Kloevekorn C, et al. Among authors: froster ug. Graefes Arch Clin Exp Ophthalmol. 2008 Oct;246(10):1441-7. doi: 10.1007/s00417-008-0836-1. Epub 2008 May 24. Graefes Arch Clin Exp Ophthalmol. 2008. PMID: 18500531

10

A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene.

Heinritz W, Grunewald S, Strenge S, Schütz A, Froster UG, Glander HJ, Paasch U, Simon JC. Heinritz W, et al. Among authors: froster ug. Br J Dermatol. 2006 May;154(5):992-4. doi: 10.1111/j.1365-2133.2006.07142.x. Br J Dermatol. 2006. PMID: 16634909 No abstract available.

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