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机译:
Abteilung Medizinische Genetik der Universität Ulm;
Abteilung Cytogenetik, Institut für Humangenetik der Universität;
机译:Clinical characterization of a patient with CNOT2 haploinsufficiency caused by a de novo partial deletion
机译:Brain MRI findings in mandibulofacial dysostosis caused by EFTUD2 haploinsufficiency: a case report with polymicrogyria and dysmorphic caudate nuclei
机译:Haploinsufficiency of AKT3 gene causing microcephaly and psychomotor delay in a patient with 1q43q44 microdeletion
机译:/ SPL Delta / -causity在广域组通信中
机译:患有Ullrich-Turner综合征的儿童和年轻人的心血管异常-经验
机译:LETm1 haploinsufficiency causes mitochondrial defects in cells from humans with Wolf-Hirschhorn syndrome: implications for dissecting the underlying pathomechanisms in this condition