A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping

American Journal of Human Genetics

Volumn 63, Issue 5, 1998, Pages 1404-1410

  Haider, Neena B ^a   Carmi, Rivka ^c   Shalev, Hana ^c   Sheffield, Val C ^a,b   Landau, Daniel ^c  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 9; CLINICAL FEATURE; FEMALE; GENE LINKAGE GROUP; GENE LOCATION; GENE LOCUS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERKALEMIA; HYPERTENSION; ISRAEL; KIDNEY FAILURE; MALE; NEPHRONOPHTHISIS; PRIORITY JOURNAL;

EID: 0032231645     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302108     Document Type: Article

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