Presymptomatic molecular diagnosis of autosomal dominant polycystic kidney disease using PKD1- and PKD2-linked markers in Cypriot families

Clinical Genetics

Volumn 50, Issue 1, 1996, Pages 10-18

  Deltas, C Constantinou ^a   Christodoulou, Kyproula ^a   Tjakouri, Chrysa ^b   Pierides, Alkis ^b  

^a CYPRUS INSTITUTE OF NEUROLOGY AND GENETICS   (Cyprus)

^b NICOSIA GENERAL HOSPITAL   (Cyprus)

Author keywords

ADPKD; Genetic heterogeneity; Linkage analysis; Molecular diagnosis; Novel mutation; Penetrance; Presymptomatic diagnosis

Indexed keywords

PROTEIN KINASE;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CHROMOSOME 16; CHROMOSOME 4; CHRONIC KIDNEY FAILURE; CONTROLLED STUDY; CYPRUS; DNA POLYMORPHISM; FEMALE; GENE LOCUS; GENE MUTATION; HAPLOTYPE; HUMAN; HUMAN CELL; INHERITANCE; KIDNEY CYST; KIDNEY POLYCYSTIC DISEASE; MAJOR CLINICAL STUDY; MALE; MARKER GENE; MOLECULAR BIOLOGY; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL;

EID: 0029819145     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb02339.x     Document Type: Article

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