Deletion 1q43 encompassing only CHRM3 in a patient with autistic disorder

European Journal of Medical Genetics

Volumn 56, Issue 2, 2013, Pages 118-122

  Petersen, Andrea Klunder ^a   Ahmad, Ausaf ^a   Shafiq, Mustafa ^a   Brown Kipphut, Brigette ^a   Fong, Chin To ^a   Anwar Iqbal, M ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

Author keywords

1q43 deletion; Acetylcholine receptor muscarinic 3; Autistic disorder; CHRM3; M3 muscarinic receptor; Microarray CGH

Indexed keywords

CHOLINERGIC RECEPTOR; MUSCARINIC M3 RECEPTOR;

AGENESIS; ARTICLE; AUTISM; CASE REPORT; CHROMOSOME 1Q; CHROMOSOME 1Q43; CHROMOSOME DELETION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HEAD CIRCUMFERENCE; HUMAN; INTELLECTUAL IMPAIRMENT; MALE; MICROCEPHALY; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PREECLAMPSIA; SEIZURE; VAGINAL DELIVERY;

AUTISTIC DISORDER; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; COMPARATIVE GENOMIC HYBRIDIZATION; GENETIC ASSOCIATION STUDIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; RECEPTOR, MUSCARINIC M3;

EID: 84873115866     PISSN: 17697212     EISSN: 18780849     Source Type: Journal    
DOI: 10.1016/j.ejmg.2012.11.003     Document Type: Article

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