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Zeitschrift Fur Rheumatologie|January 30, 2019
[Promotion of physical activity for older patients with rheumatism : Characteristics of inflammatory rheumatic diseases against the background of physical activity recommendations]A Golla, K Mattukat, W MauGenetic Epidemiology|January 17, 2002
Weighting schemes in pooled linkage analysisS Loesgen, A Dempfle, A Golla, et al.Current Opinion in Biotechnology|February 28, 2026
Advances in multiplex precision genome editing in eukaryotic and prokaryotic systemsDevin A Golla, Chunxiao Sun, Logan Haugh, et al.Clinical Genetics|March 29, 2000
Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgeryS von Gernet, A Golla, Y Ehrenfels, et al.American Journal of Medical Genetics|July 12, 1996
Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33)E Holinski-Feder, A Golla, I Rost, et al.Journal of Medical Genetics|August 1, 1997
Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis familyA Golla, P Lichmer, S von Gernet, et al.Human Genetics|July 1, 1996
Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene productD Schindelhauer, M Weiss, H Hellebrand, et al.The American Journal of Clinical Nutrition|December 1, 1981
An immunological assessment of patients with anorexia nervosaJ A Golla, L A Larson, C F Anderson, et al.Human Molecular Genetics|July 1, 1993
Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the alpha 1, beta 1, and gamma subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defectR Sudbrak, A Golla, K Hogan, et al.Pageof 3