Einträge von Elcioglu, Nursel H. auf dem Publikationsserver

Khuller, Katharina, Yigit, Gökhan, Martínez Grijalva, Carolina, Altmüller, Janine, Thiele, Holger, Nürnberg, Peter, Elcioglu, Nursel H., Yeter, Burcu, Hehr, Ute, Stein, Anja, Della Marina, Adela, Köninger, Angela, Depienne, Christel, Kaiser, Frank J., Wollnik, Bernd und Kuechler, Alma (2021) MFSD2A-associated primary microcephaly - Expanding the clinical and mutational spectrum of this ultra-rare disease. European Journal of Medical Genetics 64 (10), S. 104310. Volltext nicht vorhanden.

Schlump, Jan-Ulrich, Stein, Anja, Hehr, Ute, Karen, Tanja, Möller-Hartmann, Claudia, Elcioglu, Nursel H., Bogdanova, Nadja, Woike, Hartmut Fritz, Lohmann, Dietmar R. , Felderhoff-Mueser, Ursula, Linz, Annette und Wieczorek, Dagmar (2012) Treacher Collins syndrome: clinical implications for the paediatrician—a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature. European Journal of Pediatrics 171 (11), S. 1611-1618. Volltext nicht vorhanden.