Expanding the phenotype of mosaic trisomy 20

American Journal of Medical Genetics, Part A

Volumn 146, Issue 3, 2008, Pages 330-336

  Willis, Mary J H ^a   Bird, Lynne M ^a,b   Dell'Aquilla, Marie ^a,c   Jones, Marilyn C ^a,b  

^a UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^b RADY CHILDREN'S HOSPITAL   (United States)

^c UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

Author keywords

Mosaicism; Phenotype; Trisomy 20

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CONSTIPATION; FEMALE; HUMAN; KYPHOSIS; LEARNING DISORDER; MALE; MOSAICISM; MUSCLE HYPOTONIA; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; SPINE FUSION; TRISOMY; TRISOMY 20; VERTEBRAL CANAL STENOSIS;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; HUMANS; INFANT; MALE; MOSAICISM; PHENOTYPE; TRISOMY;

EID: 38949104197     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32126     Document Type: Article

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