Singer H - Search Results

1

Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch.

Rauch A, Hofbeck M, Leipold G, Klinge J, Trautmann U, Kirsch M, Singer H, Pfeiffer RA. Rauch A, et al. Among authors: singer h. Am J Med Genet. 1998 Jul 24;78(4):322-31. Am J Med Genet. 1998. PMID: 9714433

2

Search for somatic 22q11.2 deletions in patients with conotruncal heart defects.

Rauch A, Hofbeck M, Cesnjevar R, Koch A, Rauch R, Buheitel G, Singer H, Weyand M. Rauch A, et al. Among authors: singer h. Am J Med Genet A. 2004 Jan 15;124A(2):165-9. doi: 10.1002/ajmg.a.20323. Am J Med Genet A. 2004. PMID: 14699615

3

Monozygotic twins concordant for Cayler syndrome.

Rauch A, Hofbeck M, Bähring S, Leipold G, Trautmann U, Singer H, Pfeiffer RA. Rauch A, et al. Among authors: singer h. Am J Med Genet. 1998 Jan 6;75(1):113-7. Am J Med Genet. 1998. PMID: 9450869

4

Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries.

Hofbeck M, Rauch A, Buheitel G, Leipold G, von der Emde J, Pfeiffer R, Singer H. Hofbeck M, et al. Among authors: singer h. Heart. 1998 Feb;79(2):180-5. doi: 10.1136/hrt.79.2.180. Heart. 1998. PMID: 9538313 Free PMC article.

5

Clinical relevance of monosomy 22q11.2 in children with pulmonary atresia and ventricular septal defect.

Hofbeck M, Leipold G, Rauch A, Buheitel G, Singer H. Hofbeck M, et al. Among authors: singer h. Eur J Pediatr. 1999 Apr;158(4):302-7. doi: 10.1007/s004310051077. Eur J Pediatr. 1999. PMID: 10206128

6

Hypoparathyroidism in conotruncal heart defects.

Koch A, Hofbeck M, Buheitel G, Dörr HG, Rauch A, Rauch R, Singer H. Koch A, et al. Among authors: singer h. Eur J Pediatr. 2002 Apr;161(4):208-11. doi: 10.1007/s004310100818. Eur J Pediatr. 2002. PMID: 12014387

7

Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?

Rauch R, Rauch A, Koch A, Zink S, Kaulitz R, Girisch M, Singer H, Hofbeck M. Rauch R, et al. Among authors: singer h. Eur J Pediatr. 2004 Nov;163(11):642-5. doi: 10.1007/s00431-004-1518-6. Epub 2004 Aug 6. Eur J Pediatr. 2004. PMID: 15300432

8

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.

Rauch R, Hofbeck M, Zweier C, Koch A, Zink S, Trautmann U, Hoyer J, Kaulitz R, Singer H, Rauch A. Rauch R, et al. Among authors: singer h. J Med Genet. 2010 May;47(5):321-31. doi: 10.1136/jmg.2009.070391. Epub 2009 Nov 30. J Med Genet. 2010. PMID: 19948535 Free article.

9

A novel 22q11.2 microdeletion in DiGeorge syndrome.

Rauch A, Pfeiffer RA, Leipold G, Singer H, Tigges M, Hofbeck M. Rauch A, et al. Among authors: singer h. Am J Hum Genet. 1999 Feb;64(2):659-66. doi: 10.1086/302235. Am J Hum Genet. 1999. PMID: 9973528 Free PMC article. No abstract available.

10

Systematic assessment of atypical deletions reveals genotype-phenotype correlation in 22q11.2.

Rauch A, Zink S, Zweier C, Thiel CT, Koch A, Rauch R, Lascorz J, Hüffmeier U, Weyand M, Singer H, Hofbeck M. Rauch A, et al. Among authors: singer h. J Med Genet. 2005 Nov;42(11):871-6. doi: 10.1136/jmg.2004.030619. Epub 2005 Apr 14. J Med Genet. 2005. PMID: 15831592 Free PMC article.

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