Should the chromosome region 15q11q13 be tested systematically by FISH in the case of an autistic-like syndrome? [3]

Clinical Genetics

Volumn 61, Issue 4, 2002, Pages 310-313

  Yardin, Catherine ^a   Esclaire, F ^a   Laroche, C ^a   Terro, F ^a   Barthe, D ^a   Bonnefont, J P ^a   Gilbert, B ^a  

^a LIMOGES UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; BEHAVIOR DISORDER; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME 15Q; CHROMOSOME ANALYSIS; CHROMOSOME BAND; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME INVERSION; CHROMOSOME TRANSLOCATION; COGNITIVE DEFECT; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; FLUORESCENCE IN SITU HYBRIDIZATION; HAPPY PUPPET SYNDROME; HUMAN; INHERITANCE; LETTER; MALE; METAPHASE; PHENOTYPE; PHYSICAL EXAMINATION; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL;

AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 15; GENE DUPLICATION; GENETIC SCREENING; GENOMIC IMPRINTING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE;

EID: 0036556382     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2002.610413.x     Document Type: Letter

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