|American Journal of Human Genetics 1998 Rivka Carmi|
|A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping.(Statistical Data Included)||Biological sciences||Val C. Sheffield, Rivka Carmi, Daniel Landau, Hana Shalev, Neena B. Haider|
|Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43.||Biological sciences||Val C. Sheffield, Rivka Carmi, Ruti Parvari, Eli Herschkovitz, Adam Kanis, Rafael Gorodischer, Shlomit Shalitin|
|Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.||Biological sciences||Val C. Sheffield, Allyn L. Mark, Rivka Carmi, Brian C. Schutte, Theresa M.H. Brennan, Daniel Landau, Hana Shalev, Fred Lamb, Roxanne Y. Walder|
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