APA (7th ed.) Citation

K, B., HA, P., J, C., OLD, M., JC, M., H, E., . . . DF, C. (2004). The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene. Journal of human genetics, 49(6), 308. https://doi.org/10.1007/s10038-004-0145-4

Chicago Style (17th ed.) Citation

K, Bhalla, Phillips HA, Crawford J, McKenzie OLD, Mulley JC, Eyre H, Gardner AE, Kremmidiotis G, and Callen DF. "The De Novo Chromosome 16 Translocations of Two Patients with Abnormal Phenotypes (mental Retardation and Epilepsy) Disrupt the A2BP1 Gene." Journal of Human Genetics 49, no. 6 (2004): 308. https://doi.org/10.1007/s10038-004-0145-4.

MLA (9th ed.) Citation

K, Bhalla, et al. "The De Novo Chromosome 16 Translocations of Two Patients with Abnormal Phenotypes (mental Retardation and Epilepsy) Disrupt the A2BP1 Gene." Journal of Human Genetics, vol. 49, no. 6, 2004, p. 308, https://doi.org/10.1007/s10038-004-0145-4.