A case with a ring chromosome 22

Turkish Journal of Pediatrics

Volumn 50, Issue 2, 2008, Pages 193-196

  Koç, Altuǧ ^a   Karaer, Kadri ^a   Ergün, Mehmet Ali ^a   Yirmibeş Karaoǧuz, Meral ^a   Kan, Derya ^a   Cansu, Ali ^a   Perçin, Ferda ^a  

^a GAZI UNIVERSITY   (Turkey)

Author keywords

22q13.3 deletion syndrome; Arachnoid cyst; Autism; Dysmorphology; Ring chromosome 22

Indexed keywords

HALOPERIDOL;

ARACHNOID CYST; ARTICLE; BEHAVIOR DISORDER; CASE REPORT; CHROMOSOME 22; CHROMOSOME C BAND; CHROMOSOME DELETION; CLINICAL FEATURE; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; MALE; MENTAL DEFICIENCY; NUCLEAR MAGNETIC RESONANCE IMAGING; RING CHROMOSOME; SCHOOL CHILD; SPEECH DISORDER;

ABNORMALITIES, MULTIPLE; CHILD; CHROMOSOMES, HUMAN, PAIR 22; HUMANS; MALE; RING CHROMOSOMES;

EID: 48649084367     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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