Genetic evaluation of pervasive developmental disorders: The terminal 22q13 deletion syndrome may represent a recognizable phenotype

Clinical Genetics

Volumn 57, Issue 2, 2000, Pages 103-109

  Prasad, Chitra ^a,c   Prasad, Asuri N ^a   Chodirker, Bernard N ^a   Lee, Christine ^b   Dawson, Angelika K ^a   Jocelyn, Leslie J ^a   Chudley, Albert E ^a  

^a UNIVERSITY OF MANITOBA   (Canada)

^b IWK HEALTH CENTRE   (Canada)

^c HEALTH SCIENCES CENTRE   (Canada)

Author keywords

22q13 deletion; Developmental delay; FISH; Hypotonia; Pervasive developmental disorder

Indexed keywords

ARTICLE; BEHAVIOR; CASE REPORT; CHILD; CHILD GROWTH; CHROMOSOME 22Q; DEVELOPMENTAL DISORDER; DIGEORGE SYNDROME; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC ANALYSIS; GENETIC SCREENING; HUMAN; INFANT; MALE; MENTAL DEFICIENCY; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME; SPEECH DISORDER; VELOCARDIOFACIAL SYNDROME; WILLIAMS BEUREN SYNDROME;

AUTISTIC DISORDER; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DEVELOPMENTAL DISABILITIES; FACIES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MENTAL RETARDATION; PHENOTYPE; SYNDROME;

EID: 0033998542     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2000.570203.x     Document Type: Article

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