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American Journal of Medical Genetics. Part A|March 23, 2013
Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disabilityAnastasia Gazou, Angelika Riess, Ute Grasshoff, et al.International Journal of Medical Microbiology : IJMM|September 21, 2015
Hypoxia-inducible factor 1α modulates metabolic activity and cytokine release in anti-Aspergillus fumigatus immune responses initiated by human dendritic cellsMirjam Fliesser, Charles Oliver Morton, Michael Bonin, et al.Bioinformatics (Oxford, England)|April 17, 2013
UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarraysChristopher Schroeder, Marc Sturm, Andreas Dufke, et al.Stem Cells International|December 10, 2015
Expression of Genes Related to Germ Cell Lineage and Pluripotency in Single Cells and Colonies of Human Adult Germ Stem CellsSabine Conrad, Hossein Azizi, Maryam Hatami, et al.Acta Neuropathologica|December 14, 2006
Extradural ependymal tumor with myxopapillary and ependymoblastic differentiation in a case of Schinzel-Giedion syndromeRudi Beschorner, Manfred Wehrmann, Ulrike Ernemann, et al.American Journal of Medical Genetics. Part A|February 19, 2015
Interstitial duplication of chromosome region 1q25.1q25.3: report of a patient with mild cognitive deficits, tall stature and facial dysmorphismsMartin Kehrer, Thomas Liehr, Tanja Benkert, et al.The Journal of Molecular Diagnostics : JMD|April 12, 2008
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's diseaseChristopher Schroeder, Michael Walter, Daniela Berg, et al.Investigative Ophthalmology & Visual Science|January 26, 2007
Genome-wide expression profiling of the retinoschisin-deficient retina in early postnatal mouse developmentAndrea Gehrig, Thomas Langmann, Franziska Horling, et al.Stem Cell Research|September 10, 2013
Molecular and cell biological effects of 3,5,3'-triiodothyronine on progenitor cells of the enteric nervous system in vitroRoland Mohr, Peter Neckel, Ying Zhang, et al.Journal of Medical Genetics|July 31, 2012
Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literatureMatthias Begemann, Sabrina Spengler, Magdalena Gogiel, et al.Pageof 13