Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1p-Reference-Cited by-同舟云学术

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Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1p

Published:1998-02 Issue:2 Volume:62 Page:355-361
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Brennan Theresa M.H.,Landau Daniel,Shalev Hana,Lamb Fred,Schutte Brian C.,Walder Roxanne Y.,Mark Allyn L.,Carmi Rivka,Sheffield Val C.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Hyperplasia of the juxtaglomular complex with hyperaldosteronism and hypokalemic alkalosis;Bartter;Am J Med,1962

2. Fast and sensitive silver staining of DNA in polyacrylamide gels;Bassam;Anal Biochem,1991

3. ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family;Brandt;FEBS Lett,1995

4. Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15;Carmi;Hum Mol Genet,1995

5. Effects of furosemide and ethacrynic acid on endolymph potential in guinea pig;Chodynicki;Otolaryngol Pol,1974

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