Autistic and dysmorphic features associated with a submicroscopic 2q333-q34 interstitial deletion detected by array comparative genomic hybridization [4]

American Journal of Medical Genetics, Part A

Volumn 146, Issue 4, 2008, Pages 521-524

  Brandau, Duane T ^a   Lund, Molly ^a   Cooley, Linda D ^a   Sanger, Warren G ^b   Butler, Merlin G ^a,c  

^a UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^c CHILDREN S MERCY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; CASE REPORT; CHROMOSOME 2Q; CHROMOSOME ABERRATION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; DIAGNOSTIC VALUE; FACE DYSMORPHIA; FEEDING DISORDER; GENE DELETION; GENETIC ASSOCIATION; GROWTH DISORDER; HUMAN; INTERSTITIAL CHROMOSOME DELETION; LETTER; MALE; MICROCEPHALY; MICROGNATHIA; MUSCLE HYPOTONIA; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION;

AUTISTIC DISORDER; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 4; FACIAL ASYMMETRY; GENE EXPRESSION PROFILING; HUMANS; MALE; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; TRANSLOCATION, GENETIC;

EID: 38849143271     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32153     Document Type: Letter

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