The 15q11.2 BP1–BP2 microdeletion syndrome: A review

International Journal of Molecular Sciences

Volumn 16, Issue 2, 2015, Pages 4068-4082

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

^a UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

Author keywords

15q11.2 BP1 BP2 microdeletion; Autism; Burnside Butler syndrome; Chromosome breakpoints BP1 and BP2; Clinical and behavioral phenotype; Language and motor delays; Prader Willi and Angelman syndromes; Review

Indexed keywords

ACADEMIC ACHIEVEMENT; ATTENTION DEFICIT DISORDER; AUTISM; BEHAVIOR DISORDER; BODY DYSMORPHIC DISORDER; CHROMOSOME DELETION; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; EPILEPSY; GENOMIC INSTABILITY; GROWTH DISORDER; HUMAN; INTELLIGENCE; MEMORY DISORDER; MICROARRAY ANALYSIS; MICRODELETION SYNDROME; MINIMAL BRAIN DYSFUNCTION; PALATOPHARYNGEAL INCOMPETENCE; PARANOID PSYCHOSIS; READING; REVIEW; SCHIZOPHRENIA; SEIZURE; SPEECH DISORDER; WRITING; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; AUTISM SPECTRUM DISORDER; CHROMOSOME 15; CHROMOSOME ABERRATION; INTELLECTUAL DISABILITY; PATHOLOGY;

ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; AUTISM SPECTRUM DISORDER; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; EPILEPSY; HUMANS; INTELLECTUAL DISABILITY; SCHIZOPHRENIA;

EID: 84922900619     PISSN: 16616596     EISSN: 14220067     Source Type: Journal    
DOI: 10.3390/ijms16024068     Document Type: Review

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