Diffuse renal cystic disease in children: Morphologic and genetic correlations

Pediatric Nephrology

Volumn 12, Issue 3, 1998, Pages 173-182

  Guay Woodford, Lisa M ^a,b,g   Galliani, Carlos A ^c   Musulman Mroczek, Elizabeth ^c   Spear, Gerald S ^d   Guillot, Ann P ^e   Bernstein, Jay ^f  

^a University of Alabama at Birmingham   (United States)

^b University of Alabama at Birmingham   (United States)

^c UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF VERMONT   (United States)

^f WILLIAM BEAUMONT HOSPITAL   (United States)

^g University of Alabama at Birmingham   (United States)

Author keywords

Autosomal dominant polycystic kidney disease; Autosomal recessive polycystic kidney disease; Glomerulocystic kidney disease; Meckel syndrome; Molecular analysis; Renal cystic disease

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BILIARY TRACT MALFORMATION; CAUCASIAN; CLINICAL ARTICLE; FEMALE; FETUS; HEREDITY; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INFANT; KIDNEY POLYCYSTIC DISEASE; MALE; MOLECULAR GENETICS; MORPHOLOGY; NEGRO; NEWBORN; PRIORITY JOURNAL;

FEMALE; HUMANS; INFANT; INFANT, NEWBORN; KIDNEY; KIDNEY DISEASES, CYSTIC; MALE; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; POLYCYSTIC KIDNEY, AUTOSOMAL RECESSIVE;

EID: 0031924201     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004670050431     Document Type: Article

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