Items where Community is "CSHL labs > Hatchwell lab"

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Paper

Tegay, D. H., Lane, A. H., Roohi, J., Hatchwell, E. (March 2007) Contiguous gene deletion involving L1CAM and AVPR2 causes X-linked hydrocephalus with nephrogenic diabetes insipidus. American Journal of Medical Genetics Part A, 143A (6). pp. 594-598. ISSN 1552-4825

Herbert, M. R., Russo, J. P., Yang, S., Roohi, Jasmin, Blaxill, M., Kahler, S. G., Cremer, L., Hatchwell, Eli (2006) Autism and environmental genomics. NeuroToxicology, 27 (5). pp. 671-684. ISSN 0161813X

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

He, H., Roschke, A., Yonescu, R., Hatchwell, E., Ried, T., Kirsch, I. (November 2003) Genome-wide analysis of genetic alterations in tumor cell lines by Ccap BAC microarray. American Journal of Human Genetics, 73 (5). p. 254. ISSN 0002-9297

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

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