Clinical and genetic characterization of an autosomal dominant nephropathy

American Journal of Medical Genetics

Volumn 99, Issue 3, 2001, Pages 204-209

  Parvari, Ruti ^a   Shnaider, Alla ^b   Basok, Anna ^b   Katchko, Leonid ^b   Borochovich, Zvi ^c   Kanis, Adam ^d   Landau, Daniel ^b  

^a BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

^b BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

^c BNAI ZION MEDICAL CENTER   (Israel)

^d UNIVERSITY OF IOWA   (United States)

Author keywords

Adult onset; Autosomal dominant; Chromosome 1q21; Linkage analysis; Medullary cystic disease

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 1; CHROMOSOME 6; CHRONIC KIDNEY FAILURE; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; FAMILIAL DISEASE; FAMILY STUDY; FEMALE; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; HYPERTENSION; KIDNEY FAILURE; MALE; MEDULLARY SPONGE KIDNEY; ONSET AGE; PRIORITY JOURNAL;

ADULT; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GENES, DOMINANT; HUMANS; IRAQ; JEWS; KIDNEY; KIDNEY MEDULLA; LINKAGE (GENETICS); MALE; MIDDLE AGED; PEDIGREE; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT;

EID: 0035869098     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1158>3.0.CO;2-P     Document Type: Article

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