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American Journal of Medical Genetics|August 10, 2001
Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsiesD Sobetzko, T Sander, C M BeckerPraxis|March 21, 2002
[Early-onset generalized polyarthritis (Stickler syndrome)]J Mach, D Sobetzko, A Superti-Furga, et al.American Journal of Medical Genetics|March 4, 2000
Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individualD Sobetzko, G Eich, M Kalff-Suske, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 27, 1999
Novel GLRA1 missense mutation (P250T) in dominant hyperekplexia defines an intracellular determinant of glycine receptor channel gatingB Saul, T Kuner, D Sobetzko, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 20, 2002
Diagnosis of skeletal dysplasia by multidisciplinary assessment: a report of two cases of thanatophoric dysplasiaN Kölble, D Sobetzko, J Ersch, et al.Pageof 1