Kantarci, Sibel Publications

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping

Kantarci, Sibel

Number of items at this level: 3.

Consugar, M. B., Anderson, S. A., Rossetti, S., Pankratz, S., Ward, C. J., Torra, R., Coto, E., El-Youssef, M., Kantarci, S., Utsch, B., Hildebrandt, F., Sweeney, W. E., Avner, E. D., Torres, V. E., Cunningham, J. M., Harris, P. C. (January 2005) Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease. American Journal of Kidney Diseases, 45 (1). pp. 77-87. ISSN 0272-6386

Kantarci, S., Apak, M. Y., Eraslan, S., Nayir, A., Kayserili, H., Kirdar, B. (November 2003) Haplotype analysis in autosomal recessive polycystic kidney disease (ARPKD) families and the determination of allele frequencies of used markers in the Turkish population. American Journal of Human Genetics, 73 (5). p. 477. ISSN 0002-9297

Hatchwell, E., Tommerup, N., Kristoffersson, U., Stanyon, R., Kantarci, S. (November 2003) Joubert syndrome: a patient with a de novo t(2;22)(q13;q11.1). American Journal of Human Genetics, 73 (5). p. 566. ISSN 0002-9297

This list was generated on Wed Mar 3 13:39:47 2021 EST.
CSHL HomeAbout CSHLResearchEducationNews & FeaturesCampus & Public EventsCareersGiving