1. HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Issue 10 (18th March 2019) Authors: Kause, Franziska; Zhang, Rong; Ludwig, Michael; Schmiedeke, Eberhard; Rissmann, Anke; Thiele, Holger; Altmueller, Janine; Herms, Stefan; Hilger, Alina C.; Hildebrandt, Friedhelm; Reutter, Heiko Journal: Birth defects research Issue: Volume 111:Issue 10(2019) Page Start: 591 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 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. Issue 12 (16th August 2013) Authors: Dworschak, Gabriel C.; Draaken, Markus; Marcelis, Carlo; de Blaauw, Ivo; Pfundt, Rolph; van Rooij, Iris A.L.M.; Bartels, Enrika; Hilger, Alina; Jenetzky, Ekkehart; Schmiedeke, Eberhard; Grasshoff‐Derr, Sabine; Schmidt, Dominik; Märzheuser, Stefanie; Hosie, Stuart; Weih, Sandra; Holland‐Cunz, Stef... Journal: American journal of medical genetics Issue: Volume 161:Issue 12(2013:Dec.) Page Start: 3035 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Male infant with paternal uniparental diploidy mosaicism and a 46, XX/46, XY karyotype. Issue 11 (1st August 2019) Authors: Spier, Isabel; Engels, Hartmut; Stutte, Sonja; Reutter, Heiko; Bartels, Enrika; Matos Meder, Sarah; Begemann, Matthias; Mangold, Elisabeth; Eggermann, Thomas Journal: American journal of medical genetics Issue: Volume 179:Issue 11(2019) Page Start: 2252 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evaluation of sexual function in females with exstrophy-epispadias-complex: A survey of the multicenter German CURE-Net. Issue 2 (April 2017) Authors: Ebert, Anne-Karoline; Lange, Theresa; Reutter, Heiko; Jenetzky, Ekkehart; Stein, Raimund; Boemers, Thomas M.; Hirsch, Karin; Rösch, Wolfgang H.; Zwink, Nadine Journal: Journal of pediatric urology Issue: Volume 13:Issue 2(2017) Page Start: 183.e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An examination of the factors affecting intestinal wall integrity in newborns at birth. (1st February 2018) Authors: Bagci, Soyhan; Mensinga, Daniel; Katzer, David; Merz, Waltraut M.; Reutter, Heiko; Müller, Andreas Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 31:Number 3(2018) Page Start: 294 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Nonurgent Visits to the Pediatric Emergency Department before and during the First Peak of the COVID-19 Pandemic. (28th February 2022) Authors: Guckert, Laura; Reutter, Heiko; Saleh, Nadia; Ganschow, Rainer; Müller, Andreas; Ebach, Fabian Other Names: Mussa Alessandro Academic Editor. Journal: International journal of pediatrics Issue: Volume 2022(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax. Issue 5 (7th January 2022) Authors: Schneider, Sophia; Köllges, Ricarda; Stegmann, Jil D.; Thieme, Frederic; Hilger, Alina C.; Waffenschmidt, Lea; Fazaal, Julia; Kalanithy, Jeshurun C.; Geipel, Annegret; Strizek, Brigitte; Ludwig, Kerstin U.; Reutter, Heiko; Müller, Andreas Journal: American journal of medical genetics Issue: Volume 188:Issue 5(2022) Page Start: 1607 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Whole-Exome Sequencing in Nine Monozygotic Discordant Twins. (18th December 2015) Authors: Zhang, Rong; Thiele, Holger; Bartmann, Peter; Hilger, Alina C.; Berg, Christoph; Herberg, Ulrike; Klingmüller, Dietrich; Nürnberg, Peter; Ludwig, Michael; Reutter, Heiko Journal: Twin research and human genetics Issue: Volume 19:Number 1(2016) Page Start: 60 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Re‐sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL‐like association, and isolated anorectal malformation. Issue 10 (31st March 2022) Authors: Thiem, Corina E.; Stegmann, Jil D.; Hilger, Alina C.; Waffenschmidt, Lea; Bendixen, Charlotte; Köllges, Ricarda; Schmiedeke, Eberhard; Schäfer, Frank‐Mattias; Lacher, Martin; Kosch, Ferdinand; Grasshoff‐Derr, Sabine; Kabs, Carmen; Neser, Jörg; Jenetzky, Ekkehart; Fazaal, Julia; Schumacher, Johann... Journal: Birth defects research Issue: Volume 114:Issue 10(2022) Page Start: 478 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney Malformations. Issue 12 (30th June 2022) Authors: Kohl, Stefan; Avni, Fred E; Boor, Peter; Capone, Valentina; Clapp, William L; De Palma, Diego; Harris, Tess; Heidet, Laurence; Hilger, Alina C; Liapis, Helen; Lilien, Marc; Manzoni, Gianantonio; Montini, Giovanni; Negrisolo, Susanna; Pierrat, Marie-Jeanne; Raes, Ann; Reutter, Heiko; Schreuder, Mi... Journal: Nephrology dialysis transplantation Issue: Volume 37:Issue 12(2022) Page Start: 2351 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗