Reutter H - Search Results

1

De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformations.

Dworschak GC, Draaken M, Marcelis C, de Blaauw I, Pfundt R, van Rooij IA, Bartels E, Hilger A, Jenetzky E, Schmiedeke E, Grasshoff-Derr S, Schmidt D, Märzheuser S, Hosie S, Weih S, Holland-Cunz S, Palta M, Leonhardt J, Schäfer M, Kujath C, Rissmann A, Nöthen MM, Zwink N, Ludwig M, Reutter H. Dworschak GC, et al. Among authors: reutter h. Am J Med Genet A. 2013 Dec;161A(12):3035-41. doi: 10.1002/ajmg.a.36153. Epub 2013 Aug 16. Am J Med Genet A. 2013. PMID: 24038947

2

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

Engels H, Bosse K, Ehrbrecht A, Zahn S, Hoischen A, Propping P, Bindl L, Reutter H. Engels H, et al. Among authors: reutter h. Am J Med Genet. 2002 Aug 1;111(2):205-9. doi: 10.1002/ajmg.10560. Am J Med Genet. 2002. PMID: 12210352 Review.

3

[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.

4

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

5

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

6

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.

7

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.

8

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

9

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.

10

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.

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