Reutter HM - Search Results

1

A classic twin study of isolated gastroschisis.

Schulz AC, Stressig R, Ritgen J, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Bartmann P, Reutter HM. Schulz AC, et al. Among authors: reutter hm. Fetal Pediatr Pathol. 2012 Oct;31(5):324-30. doi: 10.3109/15513815.2012.659393. Epub 2012 Mar 20. Fetal Pediatr Pathol. 2012. PMID: 22433012 Review.

2

Seven new cases of familial isolated bladder exstrophy and epispadias complex (BEEC) and review of the literature.

Reutter H, Shapiro E, Gruen JR. Reutter H, et al. Am J Med Genet A. 2003 Jul 15;120A(2):215-21. doi: 10.1002/ajmg.a.20057. Am J Med Genet A. 2003. PMID: 12833402 Review.

3

Intestinal atresia, encephalocele, and cardiac malformations in infants with 47,XXX: Expansion of the phenotypic spectrum and a review of the literature.

Bağci S, Müller A, Franz A, Heydweiller A, Berg C, Nöthen MM, Bartmann P, Reutter H. Bağci S, et al. Fetal Diagn Ther. 2010;27(2):113-7. doi: 10.1159/000284929. Epub 2010 Feb 16. Fetal Diagn Ther. 2010. PMID: 20160426 Review.

4

Primary pulmonary hypertension, congenital heart defect, central nervous system malformations, hypo- and aplastic toes: another case of Yunis-Varón syndrome or report of a new entity.

Reutter H, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Eggermann T, Spengler S, Bartmann P, Rudnik-Schöneborn S. Reutter H, et al. Eur J Med Genet. 2012 Jan;55(1):27-31. doi: 10.1016/j.ejmg.2011.09.002. Epub 2011 Oct 11. Eur J Med Genet. 2012. PMID: 22044576

5

Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder.

Schulz AC, Bartels E, Stressig R, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Ludwig M, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Heydweiller A, Bachour H, Schumacher J, Bartmann P, Nöthen MM, Reutter H. Schulz AC, et al. Birth Defects Res A Clin Mol Teratol. 2012 Mar;94(3):182-6. doi: 10.1002/bdra.22879. Epub 2012 Jan 30. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22287212

6

Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literature.

Berner AL, Bağci S, Wohlleber E, Engels E, Müller A, Bartmann P, Weber RG, Reutter H. Berner AL, et al. Cytogenet Genome Res. 2012;136(4):308-13. doi: 10.1159/000337019. Epub 2012 Mar 17. Cytogenet Genome Res. 2012. PMID: 22433391 Review.

7

VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis.

Bartels E, Schulz AC, Mora NW, Pineda-Alvarez DE, Wijers CHW, Marcelis CM, Stressig R, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Hoffmann P, Hilger AC, Dworschak GC, Baudisch F, Ludwig M, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Bartmann P, Nöthen MM, van Rooij IALM, Solomon BD, Reutter HM. Bartels E, et al. Among authors: reutter hm. Clin Dysmorphol. 2012 Oct;21(4):191-195. doi: 10.1097/MCD.0b013e328358243c. Clin Dysmorphol. 2012. PMID: 22895008 Free PMC article.

8

CNV analysis in monozygotic twin pairs discordant for urorectal malformations.

Baudisch F, Draaken M, Bartels E, Schmiedeke E, Bagci S, Bartmann P, Nöthen MM, Ludwig M, Reutter H. Baudisch F, et al. Twin Res Hum Genet. 2013 Aug;16(4):802-7. doi: 10.1017/thg.2013.29. Epub 2013 May 9. Twin Res Hum Genet. 2013. PMID: 23659922

9

Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum.

Choinitzki V, Zwink N, Bartels E, Baudisch F, Boemers TM, Hölscher A, Turial S, Bachour H, Heydweiller A, Kurz R, Bartmann P, Pauly M, Brokmeier U, Leutner A, Nöthen MM, Schumacher J, Jenetzky E, Reutter H. Choinitzki V, et al. Birth Defects Res A Clin Mol Teratol. 2013 Dec;97(12):786-91. doi: 10.1002/bdra.23205. Epub 2013 Dec 5. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 24307608

10

Early prenatal diagnosis of the OEIS complex with different appearance in early compared with late pregnancy before spontaneous rupture of the cloacal membrane.

Mallmann MR, Reutter H, Geipel A, Berg C, Gembruch U. Mallmann MR, et al. Prenat Diagn. 2014 Aug;34(8):803-5. doi: 10.1002/pd.4355. Epub 2014 May 26. Prenat Diagn. 2014. PMID: 24623061 No abstract available.

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