Delineating the phenotype of 1p36 deletion in adolescents and adults

American Journal of Medical Genetics, Part A

Volumn 164, Issue 10, 2014, Pages 2496-2503

  Brazil, Ashley ^a,b   Stanford, Kevin ^b   Smolarek, Teresa ^a,b   Hopkin, Robert ^a,b  

^a UNIVERSITY OF CINCINNATI   (United States)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

1p36 deletion syndrome; 1pter deletion; Adolescents 1p36; Adulthood hypotonia; Adults 1p36; Cardiomyopathy 1p36; Monosomy 1p36; Speech problems 1p36

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME DELETION; CHROMOSOME DELETION 1P36; CLINICAL ARTICLE; CONGENITAL HEART MALFORMATION; FEMALE; FUNCTIONAL STATUS; HEARING IMPAIRMENT; HUMAN; MALE; MUSCLE HYPOTONIA; PHENOTYPE; QUALITY OF LIFE; SEIZURE; SPEECH; VISUAL DISORDER; CHILD; CHROMOSOME 1; CHROMOSOME DISORDER; COMPLICATION; CROSS-SECTIONAL STUDY; GENE DELETION; GENETICS; MIDDLE AGED; PATHOPHYSIOLOGY; YOUNG ADULT;

ADOLESCENT; ADULT; CHILD; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; CROSS-SECTIONAL STUDIES; FEMALE; HUMANS; MALE; MIDDLE AGED; PHENOTYPE; SEQUENCE DELETION; YOUNG ADULT;

EID: 84908232203     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36657     Document Type: Article

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