Kress W - Search Results

1

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.

Loeys BL, Chen J, Neptune ER, Judge DP, Podowski M, Holm T, Meyers J, Leitch CC, Katsanis N, Sharifi N, Xu FL, Myers LA, Spevak PJ, Cameron DE, De Backer J, Hellemans J, Chen Y, Davis EC, Webb CL, Kress W, Coucke P, Rifkin DB, De Paepe AM, Dietz HC. Loeys BL, et al. Among authors: kress w. Nat Genet. 2005 Mar;37(3):275-81. doi: 10.1038/ng1511. Epub 2005 Jan 30. Nat Genet. 2005. PMID: 15731757 Free article.

2

Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.

Kress W, Schropp C, Lieb G, Petersen B, Büsse-Ratzka M, Kunz J, Reinhart E, Schäfer WD, Sold J, Hoppe F, Pahnke J, Trusen A, Sörensen N, Krauss J, Collmann H. Kress W, et al. Eur J Hum Genet. 2006 Jan;14(1):39-48. doi: 10.1038/sj.ejhg.5201507. Eur J Hum Genet. 2006. PMID: 16251895

3

Endocardial cushion defect in a patient with Crouzon syndrome carrying a mutation in the fibroblast growth factor receptor (FGFR)-2 gene.

Schulz C, Kress W, Schömig A, Wessely R. Schulz C, et al. Among authors: kress w. Clin Genet. 2007 Oct;72(4):305-7. doi: 10.1111/j.1399-0004.2007.00861.x. Clin Genet. 2007. PMID: 17850625

4

Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses).

Kress W, Collmann H, Büsse M, Halliger-Keller B, Mueller CR. Kress W, et al. Cytogenet Cell Genet. 2000;91(1-4):134-7. doi: 10.1159/000056833. Cytogenet Cell Genet. 2000. PMID: 11173845

5

An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.

Kress W, Petersen B, Collmann H, Grimm T. Kress W, et al. Cytogenet Cell Genet. 2000;91(1-4):138-40. doi: 10.1159/000056834. Cytogenet Cell Genet. 2000. PMID: 11173846

6

Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1.

Seifert W, Holder-Espinasse M, Kühnisch J, Kahrizi K, Tzschach A, Garshasbi M, Najmabadi H, Walter Kuss A, Kress W, Laureys G, Loeys B, Brilstra E, Mancini GM, Dollfus H, Dahan K, Apse K, Hennies HC, Horn D. Seifert W, et al. Among authors: kress w. Hum Mutat. 2009 Feb;30(2):E404-20. doi: 10.1002/humu.20886. Hum Mutat. 2009. PMID: 19006247

7

Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.

Schulz AL, Albrecht B, Arici C, van der Burgt I, Buske A, Gillessen-Kaesbach G, Heller R, Horn D, Hübner CA, Korenke GC, König R, Kress W, Krüger G, Meinecke P, Mücke J, Plecko B, Rossier E, Schinzel A, Schulze A, Seemanova E, Seidel H, Spranger S, Tuysuz B, Uhrig S, Wieczorek D, Kutsche K, Zenker M. Schulz AL, et al. Among authors: kress w. Clin Genet. 2008 Jan;73(1):62-70. doi: 10.1111/j.1399-0004.2007.00931.x. Epub 2007 Nov 27. Clin Genet. 2008. PMID: 18042262

8

Terminal deletion of the long arm of chromosome 10: a new case with breakpoint in q25.3.

Petersen B, Strassburg HM, Feichtinger W, Kress W, Schmid M. Petersen B, et al. Among authors: kress w. Am J Med Genet. 1998 Apr 28;77(1):60-2. Am J Med Genet. 1998. PMID: 9557896

9

Genetic investigations of Saethre-Chotzen syndrome presenting with renal cell carcinoma.

Seifert G, Kress W, Meisel C, Henze G, Seeger K. Seifert G, et al. Among authors: kress w. Cancer Genet Cytogenet. 2006 Nov;171(1):76-8. doi: 10.1016/j.cancergencyto.2006.06.012. Cancer Genet Cytogenet. 2006. PMID: 17074596

10

Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosis.

Keupp K, Li Y, Vargel I, Hoischen A, Richardson R, Neveling K, Alanay Y, Uz E, Elcioğlu N, Rachwalski M, Kamaci S, Tunçbilek G, Akin B, Grötzinger J, Konas E, Mavili E, Müller-Newen G, Collmann H, Roscioli T, Buckley MF, Yigit G, Gilissen C, Kress W, Veltman J, Hammerschmidt M, Akarsu NA, Wollnik B. Keupp K, et al. Among authors: kress w. Mol Genet Genomic Med. 2013 Nov;1(4):223-37. doi: 10.1002/mgg3.28. Epub 2013 Aug 19. Mol Genet Genomic Med. 2013. PMID: 24498618 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

312 results

Search Page