15q13q14 deletions: Phenotypic characterization and molecular delineation by comparative genomic hybridization

American Journal of Medical Genetics, Part A

Volumn 146, Issue 15, 2008, Pages 1933-1941

  Brunetti Pierri, Nicola ^a   Sahoo, Trilochan ^a,b   Frioux, Sarah ^c   Chinault, Craig ^a,b   Zascavage, Roxanne ^a   Cheung, Sau Wai ^a,b   Peters, Sarika ^a   Shinawi, Marwan ^a,b  

^a TEXAS CHILDREN S HOSPITAL   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c TRIPLER ARMY MEDICAL CENTER   (United States)

Author keywords

15q13q14; Array CGH; Mental retardation; Prader willi Angelman syndrome

Indexed keywords

ARTICLE; BIFID UVULA; CASE REPORT; CHILD; CHROMOSOME DELETION; CHROMOSOME DELETION 13Q; CHROMOSOME DELETION 14; CHROMOSOME DELETION 15Q; CLEFT PALATE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART MALFORMATION; DNA MICROARRAY; ECHOCARDIOGRAPHY; FACE DYSMORPHIA; FEMALE; FRAGILE X SYNDROME; HAPPY PUPPET SYNDROME; HEART ATRIUM SEPTUM DEFECT; HUMAN; LEARNING DISORDER; MALE; MORPHOLOGICAL TRAIT; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PATENT FORAMEN OVALE; PHYSICAL EXAMINATION; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; CHROMOSOME 15; DEVELOPMENTAL DISORDER; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; GENOME; INFANT; PHENOTYPE; PSYCHOLOGIC TEST;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; DEVELOPMENTAL DISABILITIES; FEMALE; GENOME, HUMAN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE; PSYCHOLOGICAL TESTS;

EID: 49649105554     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32324     Document Type: Article

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