Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder

Journal of Pediatrics

Volumn 133, Issue 3, 1998, Pages 363-365

  Meyer, G A ^a   Blum, N J ^a   Hitchcock, W ^a   Fortina, P ^a  

^a NAVAL MEDICAL CENTER PORTSMOUTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTISM; CHILD; CLINICAL ARTICLE; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; FRAGILE X SYNDROME; GENE MUTATION; GENOME; HUMAN; ISOTOPE LABELING; MENTAL DEFICIENCY; NUCLEOTIDE SEQUENCE; PREVALENCE; PRIORITY JOURNAL; SOUTHERN BLOTTING; X CHROMOSOME ABERRATION;

EID: 0031709301     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(98)70270-7     Document Type: Article

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