Fetal renal anomalies and genetic syndromes

Prenatal Diagnosis

Volumn 21, Issue 11, 2001, Pages 992-1003

  Wellesley, Diana ^a   Howe, David T ^a  

^a PRINCESS ANNE HOSPITAL   (United Kingdom)

Author keywords

Diagnosis; Genetic syndromes; Investigative tests; Renal anomalies

Indexed keywords

BARDET BIEDL SYNDROME; BECKWITH WIEDEMANN SYNDROME; ELEJALDE SYNDROME; FETUS; FRASER SYNDROME; GENETIC DISORDER; HORSESHOE KIDNEY; HUMAN; HYDRONEPHROSIS; KABUKI MAKEUP SYNDROME; KIDNEY AGENESIS; KIDNEY MALFORMATION; KIDNEY POLYCYSTIC DISEASE; MECKEL SYNDROME; MENTAL RETARDATION MALFORMATION SYNDROME; MULTIPLE MALFORMATION SYNDROME; PERLMAN SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; SIMPSON GOLABI BEHMEL SYNDROME; SYNDROME VATER; URINARY TRACT MALFORMATION; ZELLWEGER SYNDROME;

ABNORMALITIES, MULTIPLE; FETAL DISEASES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; KIDNEY; KIDNEY DISEASES; SYNDROME; ULTRASONOGRAPHY, PRENATAL;

EID: 0035206869     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.209     Document Type: Review

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