Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Sabine Uhrig

Missense Variant in CCDC22 Causes X-Linked Recessive Intellectual Disability With Features of Ritscher-Schinzel/3c Syndrome

European Journal of Human Genetics

English

Multiplex-Fish for Pre- And Postnatal Diagnostic Applications

American Journal of Human Genetics

English

PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome

American Journal of Human Genetics

English