Thaker, V. V., Esteves, K. M., Towne, M. C., Brownstein, C. A., James, P. M., Crowley, L., . . . Agrawal, P. B. (2015). Whole Exome Sequencing Identifies RAI1 Mutation in a Morbidly Obese Child Diagnosed With ROHHAD Syndrome. J Clin Endocrinol Metab.
Chicago-stil citatThaker, Vidhu V., et al. "Whole Exome Sequencing Identifies RAI1 Mutation in a Morbidly Obese Child Diagnosed With ROHHAD Syndrome." J Clin Endocrinol Metab 2015.
MLA-referensThaker, Vidhu V., et al. "Whole Exome Sequencing Identifies RAI1 Mutation in a Morbidly Obese Child Diagnosed With ROHHAD Syndrome." J Clin Endocrinol Metab 2015.
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