Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndrome

American Journal of Kidney Diseases

Volumn 30, Issue 2, 1997, Pages 174-179

  Turco, Alberto E ^a   Bresin, Elena ^b   Rossetti, Sandro ^b   Peterlin, Borut ^b   Morandi, Raffaella ^b   Pignatti, Pier Franco ^b  

^a UNIVERSITY HOSPITAL OF VERONA   (Italy)

^b NONE

Author keywords

Alport's syndrome; Genetic counseling; Genetic heterogeneity; Linkage analysis; Molecular diagnosis; Prenatal diagnosis

Indexed keywords

ADULT; ALPORT SYNDROME; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHROMOSOME 2Q; DNA DETERMINATION; EYE DISEASE; FEMALE; GENE FREQUENCY; GENE LOCATION; GENE MUTATION; GENETIC LINKAGE; GLOMERULUS BASEMENT MEMBRANE; HAPLOTYPE; HEMATURIA; HUMAN; PERCEPTION DEAFNESS; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; SEX DETERMINATION;

EID: 0030841022     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0272-6386(97)90050-0     Document Type: Article

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