Angelman syndrome without detectable chromosome 15q11-13 anomaly: Clinical study of familial and isolated cases

American Journal of Medical Genetics

Volumn 76, Issue 3, 1998, Pages 262-268

  Laan, Laura A E M ^a   Halley, Dicky J J ^b   Den Boer, Annemieke Th ^a   Hennekam, Raoul C M ^c   Renier, Willy O ^d   Brouwer, Oebele F ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b ERASMUS MEDICAL CENTER   (Netherlands)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

^d RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Angelman syndrome; Clinical findings; EEG findings; Familial cases

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 15Q; CLINICAL ARTICLE; CYTOGENETICS; ELECTROENCEPHALOGRAPHY; FAMILY STUDY; FEMALE; HAPPY PUPPET SYNDROME; HUMAN; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; ANGELMAN SYNDROME; CHILD; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; HUMANS; MALE; MIDDLE AGED;

EID: 0032546297     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980319)76:3<262::AID-AJMG11>3.0.CO;2-F     Document Type: Article

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