Reutter H - Search Results

1

Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction.

Kolvenbach CM, Dworschak GC, Frese S, Japp AS, Schuster P, Wenzlitschke N, Yilmaz Ö, Lopes FM, Pryalukhin A, Schierbaum L, van der Zanden LFM, Kause F, Schneider R, Taranta-Janusz K, Szczepańska M, Pawlaczyk K, Newman WG, Beaman GM, Stuart HM, Cervellione RM, Feitz WFJ, van Rooij IALM, Schreuder MF, Steffens M, Weber S, Merz WM, Feldkötter M, Hoppe B, Thiele H, Altmüller J, Berg C, Kristiansen G, Ludwig M, Reutter H, Woolf AS, Hildebrandt F, Grote P, Zaniew M, Odermatt B, Hilger AC. Kolvenbach CM, et al. Among authors: reutter h. Am J Hum Genet. 2019 May 2;104(5):994-1006. doi: 10.1016/j.ajhg.2019.03.023. Am J Hum Genet. 2019. PMID: 31051115 Free PMC article.

2

[Genetic and molecular biological aspects of the bladder exstrophy-epispadias complex (BEEC)].

Ludwig M, Utsch B, Reutter H. Ludwig M, et al. Among authors: reutter h. Urologe A. 2005 Sep;44(9):1037-8, 1040-4. doi: 10.1007/s00120-005-0863-z. Urologe A. 2005. PMID: 15973548 Review. German.

3

MTHFR 677 TT genotype in a mother and her child with Down syndrome, atrioventricular canal and exstrophy of the bladder: implications of a mutual genetic risk factor?

Reutter H, Betz RC, Ludwig M, Boemers TM. Reutter H, et al. Eur J Pediatr. 2006 Aug;165(8):566-8. doi: 10.1007/s00431-006-0116-1. Epub 2006 Apr 7. Eur J Pediatr. 2006. PMID: 16602006

4

Bladder exstrophy-epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients.

Reutter H, Thauvin-Robinet C, Boemers TM, Rösch WH, Ludwig M. Reutter H, et al. Scand J Urol Nephrol. 2006;40(3):221-4. doi: 10.1080/00365590600621204. Scand J Urol Nephrol. 2006. PMID: 16809264

5

Bladder exstrophy and Epstein type congenital macrothrombocytopenia: evidence for a common cause?

Utsch B, DiFeo A, Kujat A, Karle S, Schuster V, Lenk H, Jacobs U, Müller M, Dötsch J, Rascher W, Reutter H, Martignetti JA, Ludwig M, Tröbs RB. Utsch B, et al. Among authors: reutter h. Am J Med Genet A. 2006 Oct 15;140(20):2251-3. doi: 10.1002/ajmg.a.31454. Am J Med Genet A. 2006. PMID: 16969870 No abstract available.

6

Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex.

Reutter H, Becker T, Ludwig M, Schäfer N, Detlefsen B, Beaudoin S, Fisch M, Ebert AK, Rösch W, Nöthen MM, Boemers TM, Betz RC. Reutter H, et al. Am J Med Genet A. 2006 Nov 15;140(22):2506-9. doi: 10.1002/ajmg.a.31484. Am J Med Genet A. 2006. PMID: 17041930 No abstract available.

7

Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.

Reutter H, Hoischen A, Ludwig M, Stein R, Radlwimmer B, Engels H, Wolffenbuttel KP, Weber RG. Reutter H, et al. BJU Int. 2007 Sep;100(3):646-50. doi: 10.1111/j.1464-410X.2007.07086.x. BJU Int. 2007. PMID: 17669146

8

Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome.

Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dötsch J, Ludwig M, Reutter H, Innis JW. Utsch B, et al. Among authors: reutter h. Am J Med Genet A. 2007 Dec 15;143A(24):3161-8. doi: 10.1002/ajmg.a.31967. Am J Med Genet A. 2007. PMID: 17935235 Free article.

9

Concordance analyses of twins with bladder exstrophy-epispadias complex suggest genetic etiology.

Reutter H, Qi L, Gearhart JP, Boemers T, Ebert AK, Rösch W, Ludwig M, Boyadjiev SA. Reutter H, et al. Am J Med Genet A. 2007 Nov 15;143A(22):2751-6. doi: 10.1002/ajmg.a.31975. Am J Med Genet A. 2007. PMID: 17937426 No abstract available.

10

Investigation of FGF10 as a candidate gene in patients with anorectal malformations and exstrophy of the cloaca.

Krüger V, Khoshvaghti M, Reutter H, Vogt H, Boemers TM, Ludwig M. Krüger V, et al. Among authors: reutter h. Pediatr Surg Int. 2008 Aug;24(8):893-7. doi: 10.1007/s00383-008-2193-x. Epub 2008 Jun 28. Pediatr Surg Int. 2008. PMID: 18587586

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