Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype.

MLA

Rubinsztein, D. C., et al. “Haplotype Analysis of the Delta 2642 and (CAG)n Polymorphisms in the Huntington’s Disease (HD) Gene Provides an Explanation for an Apparent ‘Founder’ HD Haplotype.” Human Molecular Genetics, vol. 4, no. 2, Feb. 1995, pp. 203–06. EBSCOhost, https://doi.org/10.1093/hmg/4.2.203.

APA

Rubinsztein, D. C., Leggo, J., Goodburn, S., Barton, D. E., & Ferguson-Smith, M. A. (1995). Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington’s disease (HD) gene provides an explanation for an apparent “founder” HD haplotype. Human Molecular Genetics, 4(2), 203–206. https://doi.org/10.1093/hmg/4.2.203

Chicago

Rubinsztein, D C, J Leggo, S Goodburn, D E Barton, and M A Ferguson-Smith. 1995. “Haplotype Analysis of the Delta 2642 and (CAG)n Polymorphisms in the Huntington’s Disease (HD) Gene Provides an Explanation for an Apparent ‘Founder’ HD Haplotype.” Human Molecular Genetics 4 (2): 203–6. doi:10.1093/hmg/4.2.203.