An 800 kb deletion at 17q23.2 including the MED13 (THRAP1) gene, revealed by aCGH in a patient with a SMC 17p

Inner-membrane proteins PMI/TMEM11 regulate mitochondrial morphogenesis independently of the DRP1/MFN fission/fusion pathways

(2011) Thomas Rival et al.   EMBO REPORTS

High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: Delineating novel loci for apraxia

(2009) Jillene M. Kogan et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mechanisms and Consequences of Small Supernumerary Marker Chromosomes: From Barbara McClintock to Modern Genetic-Counseling Issues

(2008) Erin L. Baldwin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The Human CDK8 Subcomplex Is a Histone Kinase That Requires Med12 for Activity and Can Function Independently of Mediator

(2008) M. T. Knuesel et al.   MOLECULAR AND CELLULAR BIOLOGY

Mediator Links Epigenetic Silencing of Neuronal Gene Expression with X-Linked Mental Retardation

(2008) Ning Ding et al.   MOLECULAR CELL

Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization

(2008) Karen D Tsuchiya et al.   Molecular Cytogenetics

TWIST microdeletion identified by array CGH in a patient presenting Saethre–Chotzen phenotype and a complex rearrangement involving chromosomes 2 and 7

(2007) Caroline Schluth-Bolard et al.   European Journal of Medical Genetics