A patient with autistic disorder and a 20/22 chromosomal translocation

Developmental Medicine and Child Neurology

Volumn 40, Issue 7, 1998, Pages 492-495

  Carratalá, Francisco ^a,c   Galan, Francisco ^b   Moya, Manuel ^c   Estivill, Xavier ^d   Pritchard, Melanie A ^d   Llevadot, Roser ^d   Nadal, Marga ^d   Gratacòs, Monica ^d  

^a Neurology Division

^b Genetics Division

^c MIGUEL HERNÁNDEZ UNIVERSITY   (Spain)

^d Institut de Recerca Oncologica   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

HEXAMETHYLPROPYLENE AMINE OXIME TECHNETIUM TC 99M;

ARTICLE; AUTISM; BRAIN PERFUSION; CASE REPORT; CHROMOSOME TRANSLOCATION 20; CHROMOSOME TRANSLOCATION 22; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; FUNNEL CHEST; HUMAN; INTELLIGENCE QUOTIENT; INTERSTITIAL CHROMOSOME DELETION; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMETRY; THUMB MALFORMATION; VERBAL BEHAVIOR;

EID: 0031815248     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1469-8749.1998.tb15400.x     Document Type: Article

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