Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region.

MLA

Male, Alison, et al. “Delineation of an Estimated 6.7 MB Candidate Interval for an Anophthalmia Gene at 3q26.33-Q28 and Description of the Syndrome Associated with Visible Chromosome Deletions of This Region.” European Journal of Human Genetics, vol. 10, no. 12, Dec. 2002, p. 807. EBSCOhost, https://doi.org/10.1038/sj.ejhg.5200890.

APA

Male, A., Davies, A., Bergbaum, A., Keeling, J., FitzPatrick, D., Ogilvie, C. M., & Berg, J. (2002). Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region. European Journal of Human Genetics, 10(12), 807. https://doi.org/10.1038/sj.ejhg.5200890

Chicago

Male, Alison, Angela Davies, Anne Bergbaum, Jean Keeling, David FitzPatrick, Caroline Mackie Ogilvie, and Jonathan Berg. 2002. “Delineation of an Estimated 6.7 MB Candidate Interval for an Anophthalmia Gene at 3q26.33-Q28 and Description of the Syndrome Associated with Visible Chromosome Deletions of This Region.” European Journal of Human Genetics 10 (12): 807. doi:10.1038/sj.ejhg.5200890.