1. 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) ↗
2. 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) ↗