American Journal of Human Genetics 1998 Val C. Sheffield - Abstracts
| American Journal of Human Genetics 1998 Val C. Sheffield | |||||
| Title | Subject | Authors | |||
|---|---|---|---|---|---|
| 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 | |||
| Comprehensive human genetic maps: individual and sex-specfic variation in recombination. | Biological sciences | Val C. Sheffield, Jeffrey C. Murray, Raymond L. White, Karl W. Broman, James L. Weber | |||
| 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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