Συγγραφείς:
Manolakos, E.
Vetro, A.
Kefalas, K.
Thomaidis, L.
Aperis, G.
Sotiriou, S.
Kitsos, G.
Merkas, M.
Sifakis, S.
Papoulidis, I.
Liehr, T.
Zuffardi, O.
Petersen, M.B.
Λέξεις-κλειδιά:
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
