Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies

Journal of Clinical Investigation

Volumn 91, Issue 6, 1993, Pages 2351-2357

  Scheinman, S J ^a   Pook, M A ^a   Wooding, C ^a   Pang, J T ^a   Frymoyer, P A ^a   Thakker, R V ^a  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

Author keywords

DNA linkage studies; Fanconi syndrome; X linked recessive nephrolithiasis

Indexed keywords

PRIMER DNA;

ADULT; AGED; ARTICLE; CHROMOSOME XP; CLINICAL ARTICLE; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; GENETIC MARKER; HUMAN; KIDNEY FAILURE; KIDNEY TUBULE DISORDER; KIDNEY TUBULE FUNCTION; MALE; MOLECULAR CLONING; NEPHROLITHIASIS; PRESCHOOL CHILD; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; X CHROMOSOME RECESSIVE INHERITANCE;

EID: 0027177179     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI116467     Document Type: Article

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