No evidence for submicroscopic 22qter deletions in patients with features suggestive for Angelman syndrome

American Journal of Medical Genetics

Volumn 109, Issue 2, 2002, Pages 117-120

  De Vries, Bert B A ^a,b   Tyson, Jess ^a   Winter, Robin M ^a   Malcolm, Sue ^a,c  

^a GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^b ERASMUS MEDICAL CENTER   (Netherlands)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

22qter deletions; Angelman syndrome; Mental retardation

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL EXAMINATION; FEMALE; GENE FREQUENCY; HAPPY PUPPET SYNDROME; HUMAN; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; SYNDROME DELINEATION;

ADOLESCENT; ADULT; ANGELMAN SYNDROME; BLOTTING, SOUTHERN; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DNA; FAMILY HEALTH; FEMALE; HUMANS; INFANT; MALE; MICROSATELLITE REPEATS; PEDIGREE;

EID: 0037156330     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10318     Document Type: Article

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