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4 Einträge gefunden

Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor Suppressor
2016 - Forschungsinformationssystem des UKE
Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics
2013 - Forschungsinformationssystem des UKE - frei zugänglich
Hybrid neurofibroma/schwannoma is overrepresented among schwannomatosis and neurofibromatosis patients.
2012 - Forschungsinformationssystem des UKE
The face of Noonan syndrome: Does phenotype predict genotype.
2010 - Forschungsinformationssystem des UKE