Strenge S - Search Results

1

Pulmonary artery sling and congenital tracheal stenosis in another patient with Mowat-Wilson syndrome.

Strenge S, Heinritz W, Zweier C, Rauch A, Rolle U, Merkenschlager A, Froster UG. Strenge S, et al. Am J Med Genet A. 2007 Jul 1;143A(13):1528-30. doi: 10.1002/ajmg.a.31801. Am J Med Genet A. 2007. PMID: 17567886 No abstract available.

2

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: strenge s. 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

3

Diaphragmatic hernia in 18p- syndrome.

Strenge S, Froster UG. Strenge S, et al. Am J Med Genet A. 2004 Feb 15;125A(1):97-9. doi: 10.1002/ajmg.a.20459. Am J Med Genet A. 2004. PMID: 14755475 Review. No abstract available.

4

Renal malformations in deletion 22q11.2 patients.

Kujat A, Schulz MD, Strenge S, Froster UG. Kujat A, et al. Among authors: strenge s. Am J Med Genet A. 2006 Jul 15;140(14):1601-2. doi: 10.1002/ajmg.a.31289. Am J Med Genet A. 2006. PMID: 16761295 No abstract available.

5

A microdeletion 22q11.2 can resemble Shprintzen-Goldberg omphalocele syndrome.

Strenge S, Kujat A, Zelante L, Froster UG. Strenge S, et al. Am J Med Genet A. 2006 Dec 15;140(24):2838-9. doi: 10.1002/ajmg.a.31534. Am J Med Genet A. 2006. PMID: 17103454 No abstract available.

6

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

Strenge S, Froster UG. Strenge S, et al. 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

7

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: strenge s. Onkologie. 2008 Nov;31(11):625-8. doi: 10.1159/000162284. Epub 2008 Oct 27. Onkologie. 2008. PMID: 19145097

8

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: strenge s. 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

9

[Muscular hypotonia, developmental retardation, speech delay and mildly dysmorphic features: 22q13 deletion syndrome (Phelan-McDermid Syndrome) as an important differential diagnosis].

Strenge S, Froster UG, Kujat A, Bernhard M, Merkenschlager A. Strenge S, et al. Klin Padiatr. 2008 Sep-Oct;220(5):318-20. doi: 10.1055/s-2007-977733. Klin Padiatr. 2008. PMID: 18814345 German.

10

Instability in the normal CTG repeat range at the myotonic dystrophy locus.

Meiner A, Thamm B, Strenge S, Froster U. Meiner A, et al. Among authors: strenge s. J Med Genet. 1998 Sep;35(9):791. doi: 10.1136/jmg.35.9.791. J Med Genet. 1998. PMID: 9733048 Free PMC article. No abstract available.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

18 results

Search Page

Filters