Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15

Pediatric Neurology

Volumn 41, Issue 1, 2009, Pages 65-67

  Jovanović Privrodski, Jadranka D ^a   Kavečan, Ivana I ^a   Obrenović, Milan R ^a   Buonadonna, Lucia A ^b   Bukvić, Nenad M ^c  

^a UNIVERSITY OF NOVI SAD   (Serbia)

^b POLICLINICO   (Italy)

^c Hospital of Foggia   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; SMALL NUCLEAR RIBONUCLEOPROTEIN; VALPROIC ACID;

AGGRESSION; ARTICLE; AUTISM; BEHAVIOR DISORDER; BRACHYCEPHALY; BRAIN VENTRICLE DILATATION; CASE REPORT; CHILD; CHROMOSOME 15; CHROMOSOME ANALYSIS; CLINODACTYLY; COMPUTER ASSISTED TOMOGRAPHY; CORPUS CALLOSUM AGENESIS; CRYPTORCHISM; DEVELOPMENTAL DISORDER; EAR MALFORMATION; ELECTROENCEPHALOGRAPHY; EUCHROMATIN; FLATFOOT; FUNNEL CHEST; GROWTH RETARDATION; HUMAN; HYPERACTIVITY; HYPERTELORISM; KARYOTYPE; KARYOTYPING; MALE; MALOCCLUSION; MARKER CHROMOSOME; MENTAL DEFICIENCY; MICROCEPHALY; MICROGNATHIA; NEUROLOGIC EXAMINATION; PALATE MALFORMATION; PALPEBRAL FISSURE; PRIORITY JOURNAL; PTOSIS; SCHOOL CHILD; SEIZURE; SPEECH DISORDER; SUPERNUMERARY CHROMOSOME; TOOTH MALFORMATION;

AUTISTIC DISORDER; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; CORPUS CALLOSUM; DEVELOPMENTAL DISABILITIES; DISEASES IN TWINS; FACE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; NERVOUS SYSTEM MALFORMATIONS; SEIZURES;

EID: 66449083833     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2009.02.004     Document Type: Article

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