Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopia

Pediatric Neurology

Volumn 45, Issue 4, 2011, Pages 274-278

  Descartes, Maria ^a   Mikhail, Fady M ^a   Franklin, Judith C ^a   McGrath, Tony M ^b   Bebin, Martina ^c  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^b University of Alabama at Birmingham   (United States)

^c UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUDIOGRAPHY; BRACHYCEPHALY; BRADYCARDIA; BRANCHIOGENIC CYST; CASE REPORT; CHROMOSOME 19P; CHROMOSOME 1P; CHROMOSOME DELETION; CHROMOSOME SEGREGATION; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONDUCTION DEAFNESS; FAILURE TO THRIVE; GASTROESOPHAGEAL REFLUX; GENOME ANALYSIS; HUMAN; HYPOPLASIA; INFANT; MALE; MONOSOMY; MULTIPLE MALFORMATION SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; PERIVENTRICULAR HETEROTOPIA; POLYSOMNOGRAPHY; PRIORITY JOURNAL; RETROGNATHIA; SEIZURE; SLEEP APNEA SYNDROME; TRACHEOSTOMY; TRISOMY;

CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 19; HUMANS; INFANT; MALE; PERIVENTRICULAR NODULAR HETEROTOPIA; TRISOMY;

EID: 80052728425     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2011.06.002     Document Type: Article

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