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Journal article
Mehraein, Yasmin; Pfob, Martina; Steinlein, Ortrud K.; Aichinger, Eric; Eggert, Marlene; Bubendorff, Valerie; Mannhart, Adelina und Müller, Stefan
(2015):
2q37.3 Deletion Syndrome: Two Cases with Highly Distinctive Facial Phenotype, Discordant Association with Schizophrenic Psychosis, and Shared Deletion Breakpoint Region on 2q37.3.
In: Cytogenetic and Genome Research, Vol. 146, No. 1: pp. 33-38
[PDF, 405kB]
Steinlein, Ortrud K.; Aichinger, Eric; Trucks, Holger und Sander, Thomas
(2011):
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta.
In: BMC Medical Genetics
12:152
[PDF, 562kB]