Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review

American Journal of Medical Genetics, Part A

Volumn 152 A, Issue 10, 2010, Pages 2459-2467

  Quintero Rivera, Fabiola ^a   Sharifi Hannauer, Pantea ^b   Martinez Agosto, Julian A ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

3q29 microdeletion; Array CGH; Autism; Chromosomal microarray analysis; DLG1; FBX045; Intellectual disability; Mental retardation; PAK2; Psychosis

Indexed keywords

DNA; GUANYLATE KINASE; P21 ACTIVATED KINASE 2; UBIQUITIN PROTEIN LIGASE; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

ADOLESCENT; AGGRESSIVENESS; ANXIETY; ARTICLE; AUTISM; BIPOLAR DISORDER; CASE REPORT; CHILD; CHROMOSOME 3Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; DISEASE ASSOCIATION; DNA MICROARRAY; FACE ASYMMETRY; FACE DYSMORPHIA; FEMALE; FINGER MALFORMATION; GENETIC ANALYSIS; GENETIC SCREENING; HUMAN; INTELLECTUAL IMPAIRMENT; MALE; MENTAL DEFICIENCY; PATHOGENESIS; PHENOTYPE; POSTSYNAPTIC POTENTIAL; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SUICIDAL IDEATION; TOOTH MALFORMATION; ADULT; CHROMOSOME 3; CHROMOSOME MAP; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETICS; PATERNAL AGE; PHYSIOLOGY; PSYCHOSIS; REVIEW; SYNAPSE; SYNDROME;

ADOLESCENT; ADULT; AUTISTIC DISORDER; BIPOLAR DISORDER; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MENTAL RETARDATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PATERNAL AGE; PHENOTYPE; PSYCHOTIC DISORDERS; PTEN PHOSPHOHYDROLASE; SEQUENCE DELETION; SYNAPSES; SYNDROME;

EID: 77957895378     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33573     Document Type: Article

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