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Clinical Genetics|June 18, 2004
New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 geneK Zerres, J Senderek, S Rudnik-Schöneborn, et al.
Neuroimage|June 6, 2009
Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individualsV Markov, A Krug, S Krach, et al.
Clinical Genetics|May 14, 2016
NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS featuresJ Sachwitz, R Meyer, G Fekete, et al.
Clinical Genetics|February 23, 2018
Molecular and clinical studies in 8 patients with Temple syndromeG Gillessen-Kaesbach, B Albrecht, T Eggermann, et al.
Clinical Genetics|July 2, 2016
Recent Advances in Imprinting DisordersL Soellner, M Begemann, D J G Mackay, et al.
Clinical Genetics|August 27, 2010
Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissuesM Begemann, S Spengler, D Kanber, et al.
Psychological Medicine|November 17, 2010
Effects of a CACNA1C genotype on attention networks in healthy individualsM Thimm, T Kircher, T Kellermann, et al.
Clinical Nephrology|June 5, 2003
Genetic variations of the SLC7A9 gene: allele distribution of 13 polymorphic sites in German cystinuria patients and controlsC Schmidt, J Tomiuk, E Botzenhart, et al.
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