Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts.

MLA

Oseni, Ganiyu O., et al. “Identification of Paternal Uniparental Disomy on Chromosome 22 and a de Novo Deletion on Chromosome 18 in Individuals with Orofacial Clefts.” Molecular Genetics & Genomic Medicine, vol. 6, no. 6, Nov. 2018, pp. 924–32. EBSCOhost, https://doi.org/10.1002/mgg3.459.

APA

Oseni, G. O., Jain, D., Mossey, P. A., Busch, T. D., Gowans, L. J. J., Eshete, M. A., Adeyemo, W. L., Laurie, C. A., Laurie, C. C., Owais, A., Olaitan, P. B., Aregbesola, B. S., Oginni, F. O., Bello, S. A., Donkor, P., Audu, R., Onwuamah, C., Obiri-Yeboah, S., Plange-Rhule, G., … Butali, A. (2018). Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts. Molecular Genetics & Genomic Medicine, 6(6), 924–932. https://doi.org/10.1002/mgg3.459

Chicago

Oseni, Ganiyu O, Deepti Jain, Peter A Mossey, Tamara D Busch, Lord J J Gowans, Mekonen A Eshete, Wasiu L Adeyemo, et al. 2018. “Identification of Paternal Uniparental Disomy on Chromosome 22 and a de Novo Deletion on Chromosome 18 in Individuals with Orofacial Clefts.” Molecular Genetics & Genomic Medicine 6 (6): 924–32. doi:10.1002/mgg3.459.