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Publications by Aichinger, Eric

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Number of items: 2.

Journal article

Mehraein, Yasmin; Pfob, Martina; Steinlein, Ortrud K.; Aichinger, Eric; Eggert, Marlene; Bubendorff, Valerie; Mannhart, Adelina; 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; Sander, Thomas (2011): Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta. In: BMC Medical Genetics 12:152 [PDF, 562kB]

This list was generated on Tue Dec 1 01:30:01 2020 CET.