The Smith-Magenis syndrome: A new case with infant spasms

Minerva Pediatrica

Volumn 51, Issue 3, 1999, Pages 65-71

  Roccella, M ^a   Parisi, L ^a  

^a NONE

Author keywords

Chromosome deletion; Chromosomes, human, pair 17; Craniofacial abnormalities; Menalt retardation; Smith Magenis syndrome; Spasms, infantile

Indexed keywords

ARTICLE; BRAIN; CASE REPORT; CHROMOSOME 17; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DISORDER; COMPUTER ASSISTED TOMOGRAPHY; CRANIOFACIAL MALFORMATION; FEMALE; GENETICS; HUMAN; INFANT; INFANTILE SPASM; MENTAL DEFICIENCY; PSYCHOMOTOR DISORDER; RADIOGRAPHY; SYNDROME;

BRAIN; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 17; CRANIOFACIAL ABNORMALITIES; FEMALE; HUMANS; INFANT; MENTAL RETARDATION; PSYCHOMOTOR DISORDERS; SPASMS, INFANTILE; SYNDROME; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0033091887     PISSN: 00264946     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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