Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease

The Lancet

Volumn 340, Issue 8831, 1992, Pages 1330-1333

  Ravine, D ^a   Forrest, S M ^a   Sheffield, L J ^a   Danks, D M ^a   Walker, R G ^b   Kincaid Smith, P ^b   Gibson, R N ^b  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

^b ROYAL MELBOURNE HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENETIC HETEROGENEITY; GENOTYPE; HUMAN; KIDNEY POLYCYSTIC DISEASE; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; UNITED KINGDOM;

ADOLESCENT; ADULT; AGE FACTORS; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; DIAGNOSIS, DIFFERENTIAL; EVALUATION STUDIES; GENOTYPE; HUMAN; INFANT; MEIOSIS; MIDDLE AGE; MUTATION; PEDIGREE; PHENOTYPE; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; POLYMORPHISM (GENETICS); PREVALENCE; RECOMBINATION, GENETIC; SENSITIVITY AND SPECIFICITY; SUPPORT, NON-U.S. GOV'T; SURVIVAL RATE; VICTORIA;

EID: 0026478608     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/0140-6736(92)92503-8     Document Type: Article

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