A clinical case report and literature review of the 3q29 microdeletion syndrome

Clinical Dysmorphology

Volumn 24, Issue 3, 2015, Pages 89-94

  Cox, Devin M ^a   Butler, Merlin G ^a  

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

Author keywords

3q29 microdeletion syndrome; literature review; microarray; phenotype

Indexed keywords

3Q29 MICRODELETION SYNDROME; ADOLESCENT; AGGRESSION; ANXIETY DISORDER; CASE REPORT; CHROMOSOME DELETION; DEPRESSION; FLUORESCENCE IN SITU HYBRIDIZATION; FRONTAL BOSSING; HIGH ARCHED PALATE; HUMAN; INTELLECTUAL IMPAIRMENT; INTELLIGENCE QUOTIENT; LOGORRHEA; MALE; MICROARRAY ANALYSIS; MICROGNATHIA; OBSESSIVE COMPULSIVE DISORDER; PRIORITY JOURNAL; REVIEW; SCOLIOSIS; SPEECH DELAY; TORSION; AUTISM; CHROMOSOME 3; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; GENETIC ASSOCIATION STUDY; GENETICS; MUSCULOSKELETAL SYSTEM MALFORMATION;

ADOLESCENT; AUTISM SPECTRUM DISORDER; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 3; CRANIOFACIAL ABNORMALITIES; DEVELOPMENTAL DISABILITIES; GENETIC ASSOCIATION STUDIES; HUMANS; INTELLECTUAL DISABILITY; MALE; MUSCULOSKELETAL ABNORMALITIES;

EID: 84931346687     PISSN: 09628827     EISSN: 14735717     Source Type: Journal    
DOI: 10.1097/MCD.0000000000000077     Document Type: Review

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