3 results for author:"Obermannova B." in Literature citations
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| Mutations and pituitary morphology in a series of 82 patients with PROP1 gene defects. Obermannova B., Pfaeffle R., Zygmunt-Gorska A., Starzyk J., Verkauskiene R., Smetanina N., Bezlepkina O., Peterkova V., Frisch H., Cinek O. et al. Horm Res Paediatr 76:348-354(2011) · Mapped (1) |
| Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). Boesgaard T.W., Pruhova S., Andersson E.A., Cinek O., Obermannova B., Lauenborg J., Damm P., Bergholdt R., Pociot F., Pisinger C. et al. |
| Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene. Obermannova B., Banghova K., Sumnik Z., Dvorakova H.M., Betka J., Fencl F., Kolouskova S., Cinek O., Lebl J. Eur. J. Pediatr. 168:569-573(2009) · Mapped (9) |