@article{3090543,
    title = "Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation",
    author = "Manolakos, E. and Vetro, A. and Kefalas, K. and Thomaidis, L. and Aperis, G. and Sotiriou, S. and Kitsos, G. and Merkas, M. and Sifakis, S. and Papoulidis, I. and Liehr, T. and Zuffardi, O. and Petersen, M.B.",
    journal = "American Journal of Medical Genetics. Part A",
    year = "2011",
    volume = "155",
    number = "6",
    pages = "1476-1482",
    issn = "1552-4825, 1552-4833",
    doi = "10.1002/ajmg.a.33981",
    keywords = "autism;  brain ventricle dilatation;  case report;  child;  chromosome 2q;  chromosome deletion;  comparative genomic hybridization;  controlled study;  face dysmorphia;  female;  human;  hypertelorism;  hypoglycemia;  letter;  mental deficiency;  microcephaly;  muscle hypotonia;  newborn;  nuclear magnetic resonance imaging;  occupational therapy;  phenotype;  preschool child;  priority journal;  speech disorder;  speech therapy, Abnormalities, Multiple;  Child, Preschool;  Chromosome Deletion;  Chromosomes, Human, Pair 2;  Comparative Genomic Hybridization;  Female;  Humans;  In Situ Hybridization, Fluorescence;  Karyotyping;  Mental Retardation;  Microcephaly;  Phenotype"
}