Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene.

MLA

Popovic, Maja, et al. “Fine Mapping of the Locus for Shwachman-Diamond Syndrome at 7q11, Identification of Shared Disease Haplotypes, and Exclusion of TPST1 as a Candidate Gene.” European Journal of Human Genetics : EJHG, vol. 10, no. 4, Apr. 2002, pp. 250–58. EBSCOhost, https://doi.org/10.1038/sj.ejhg.5200798.

APA

Popovic, M., Goobie, S., Morrison, J., Ellis, L., Ehtesham, N., Richards, N., Boocock, G., Durie, P. R., & Rommens, J. M. (2002). Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene. European Journal of Human Genetics : EJHG, 10(4), 250–258. https://doi.org/10.1038/sj.ejhg.5200798

Chicago

Popovic, Maja, Sharan Goobie, Jodi Morrison, Lynda Ellis, Nadia Ehtesham, Nicole Richards, Graeme Boocock, Peter R Durie, and Johanna M Rommens. 2002. “Fine Mapping of the Locus for Shwachman-Diamond Syndrome at 7q11, Identification of Shared Disease Haplotypes, and Exclusion of TPST1 as a Candidate Gene.” European Journal of Human Genetics : EJHG 10 (4): 250–58. doi:10.1038/sj.ejhg.5200798.