Congenital diaphragmatic hernia in WAGR syndrome

American Journal of Medical Genetics

Volumn 134 A, Issue 4, 2005, Pages 430-433

  Scott, Daryl A ^a,b,c   Cooper, M L ^a   Stankiewicz, P ^a   Patel, A ^a   Potocki, L ^a,b   Cheung, S W ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b TEXAS CHILDREN S HOSPITAL   (United States)

^c NONE   (United States)

Author keywords

Chromosome 11p13; Congenital diaphragmatic hernia; WAGR; WT1

Indexed keywords

ARTICLE; BOCHDALEK HERNIA; CASE REPORT; CHROMOSOME 11P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CONGENITAL DIAPHRAGM HERNIA; DENYS DRASH SYNDROME; DIAPHRAGM; DISEASE ASSOCIATION; EMBRYO DEVELOPMENT; FLUORESCENCE IN SITU HYBRIDIZATION; FRASER SYNDROME; GENE; GENE DELETION; GENE EXPRESSION; GENE MUTATION; HUMAN; INFANT; MALE; PAX6 GENE; PRIORITY JOURNAL; UROGENITAL SYSTEM; WAGR SYNDROME; WT1 GENE;

ABNORMALITIES, MULTIPLE; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 11; EYE PROTEINS; GENE DELETION; HERNIA, DIAPHRAGMATIC; HOMEODOMAIN PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; PAIRED BOX TRANSCRIPTION FACTORS; REPRESSOR PROTEINS; WAGR SYNDROME; WT1 PROTEINS;

MAMMALIA;

EID: 18044367352     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30654     Document Type: Article

References (14)

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