APA-referens

Cao, X., Eu, K. W., Kumarasinghe, M. P., Li, H. H., Loi, C., & Cheah, P. Y. (2006). Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high‐density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function. BMJ Group.

Chicago-stil citat

Cao, X., K W. Eu, M P. Kumarasinghe, H H. Li, C. Loi, och P Y. Cheah. Mapping of Hereditary Mixed Polyposis Syndrome (HMPS) to Chromosome 10q23 By Genomewide High‐density Single Nucleotide Polymorphism (SNP) Scan and Identification of BMPR1A Loss of Function. BMJ Group, 2006.

MLA-referens

Cao, X., et al. Mapping of Hereditary Mixed Polyposis Syndrome (HMPS) to Chromosome 10q23 By Genomewide High‐density Single Nucleotide Polymorphism (SNP) Scan and Identification of BMPR1A Loss of Function. BMJ Group, 2006.

Varning: dessa hänvisningar är inte alltid fullständigt riktiga.