1. Aberrant COL11A1 splicing causes prelingual autosomal dominant nonsyndromic hearing loss in the DFNA37 locus. Issue 1 (11th November 2020) Authors: Rad, Aboulfazl; Schade‐Mann, Thore; Gamerdinger, Philipp; Yanus, Grigoriy A.; Schulte, Björn; Müller, Marcus; Imyanitov, Evgeny N.; Biskup, Saskia; Löwenheim, Hubert; Tropitzsch, Anke; Vona, Barbara Journal: Human mutation Issue: Volume 42:Issue 1(2021) Page Start: 25 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. High prevalence of GPRC5A germline mutations in BRCA1‐mutant breast cancer patients. Issue 10 (27th January 2014) Authors: Sokolenko, Anna P.; Bulanova, Daria R.; Iyevleva, Aglaya G.; Aleksakhina, Svetlana N.; Preobrazhenskaya, Elena V.; Ivantsov, Alexandr O.; Kuligina, Ekatherina Sh.; Mitiushkina, Natalia V.; Suspitsin, Evgeny N.; Yanus, Grigoriy A.; Zaitseva, Olga A.; Yatsuk, Olga S.; Togo, Alexandr V.; Kota, Pooji... Journal: International journal of cancer Issue: Volume 134:Issue 10(2014:May 15) Page Start: 2352 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗