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Physical Review Letters|April 20, 2004
Quasiparticle line shape of Sr2RuO4 and its relation to anisotropic transportS-C Wang, H-B Yang, A K P Sekharan, et al.Diagnostic and Interventional Radiology (Ankara, Turkey)|August 24, 2017
Irreversible electroporation for the treatment of localized prostate cancer: a summary of imaging findings and treatment feedbackMatthijs J Scheltema, Arnoud W Postema, Daniel M de Bruin, et al.Human Molecular Genetics|November 11, 1999
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephalyL Nanni, J E Ming, M Bocian, et al.Nature|September 21, 2001
Microscopic electronic inhomogeneity in the high-Tc superconductor Bi2Sr2CaCu2O8+xS H Pan, J P O'Neal, R L Badzey, et al.Journal of Medical Genetics|May 2, 2006
Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndromeW Seifert, M Holder-Espinasse, S Spranger, et al.Radiology|August 29, 2003
Discrimination of prostate cancer from normal peripheral zone and central gland tissue by using dynamic contrast-enhanced MR imagingMarc R Engelbrecht, Henkjan J Huisman, Robert J F Laheij, et al.Langenbeck'S Archives of Surgery|January 20, 2018
Modern work-up and extended resection in perihilar cholangiocarcinoma: the AMC experienceF Rassam, E Roos, K P van Lienden, et al.Human Molecular Genetics|August 11, 1999
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndromeM Kalff-Suske, A Wild, J Topp, et al.Clinical Genetics|November 29, 2007
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndromeA L Schulz, B Albrecht, C Arici, et al.American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.Pageof 14