Antenatal Bartter syndrome with sensorineural deafness: Refinement of the locus on chromosome 1p31

Nephrology Dialysis Transplantation

Volumn 15, Issue 7, 2000, Pages 970-974

  Vollmer, Martin ^a   Jeck, Nikola ^b   Lemmink, Henny H ^c   Vargas, Rosa ^d   Feldmann, Delphine ^e   Konrad, Martin ^b   Beekmann, Frank ^a   Van Den Heuvel, Lambertus P W J ^c   Deschenes, Georges ^e   Guay Woodford, Lisa M ^f   Antignac, Corinne ^d   Seyberth, Hannsjörg W ^b   Hildebrandt, Friedhelm ^a   Knoers, Nine V A M ^c,g  

^a UNIVERSITY OF FREIBURG   (Germany)

^b UNIVERSITY HOSPITAL MARBURG   (Germany)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d INSERM   (France)

^e Depts Biochem Pediat N   (France)

^f UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^g RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

Author keywords

Antenatal Bartter syndrome; Chromosome 1p31; Deafness; Haplotype analysis

Indexed keywords

ARTICLE; BARTTER SYNDROME; CHILD; CHROMOSOME 1P; CLINICAL ARTICLE; CLINICAL TRIAL; CONSANGUINITY; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; HUMAN CELL; MALE; PERCEPTION DEAFNESS; PRIORITY JOURNAL;

EID: 0034047910     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/15.7.970     Document Type: Article

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