Deletion of hepatocyte nuclear factor-1-beta in an infant with prune belly syndrome

American Journal of Perinatology

Volumn 27, Issue 7, 2010, Pages 559-563

  Haeri, Sina ^a   Devers, Patricia L ^a   Kaiser Rogers, Kathleen A ^a   Moylan, Vincent J ^a   Torchia, Beth S ^b   Horton, Amanda L ^a   Wolfe, Honor M ^a   Aylsworth, Arthur S ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^b PerkinElmer   (United States)

Author keywords

CGH; chromosome 17q; Eagle Barrett syndrome; Fr hlich's syndrome; HNF1B; Obrinsky syndrome; Prune belly syndrome; TCF2; triad syndrome; vHnf1

Indexed keywords

HEPATOCYTE NUCLEAR FACTOR 1BETA; TRANSCRIPTION FACTOR;

ABDOMINAL DISTENSION; ARTICLE; CASE REPORT; CLINICAL FEATURE; CRYPTORCHISM; GENE DELETION; GENE EXPRESSION; GENE MUTATION; HUMAN; INFANT; KIDNEY TUBULE; LUNG HYPOPLASIA; MUELLERIAN DUCT; OBSTRUCTIVE UROPATHY; PHENOTYPE; PRIORITY JOURNAL; PRUNE BELLY SYNDROME; RESPIRATORY ARREST; RESPIRATORY DISTRESS; TISSUE SPECIFICITY; URINARY TRACT DISEASE; CHROMOSOME 17; CHROMOSOME DELETION; CONGENITAL MALFORMATION; ECHOGRAPHY; ECHOMAMMOGRAPHY; FATALITY; FEMALE; FETUS DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; KIDNEY; MALE; NEWBORN; OLIGOHYDRAMNIOS; PATHOLOGY; PREGNANCY; PROSTATE; URETHRA;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; FATAL OUTCOME; FEMALE; FETAL DISEASES; HEPATOCYTE NUCLEAR FACTOR 1-BETA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KIDNEY; MALE; OLIGOHYDRAMNIOS; PREGNANCY; PROSTATE; PRUNE BELLY SYNDROME; ULTRASONOGRAPHY, MAMMARY; URETHRA;

EID: 77954880589     PISSN: 07351631     EISSN: 10988785     Source Type: Journal    
DOI: 10.1055/s-0030-1248943     Document Type: Article

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