APA Zitierstil

Vervoort, V., Viljoen, D., Smart, R., Suthers, G., DuPont, B., Abbott, A., & Schwartz, C. (2002). Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype. BMJ Group.

Chicago Zitierstil

Vervoort, V., D. Viljoen, R. Smart, G. Suthers, B. DuPont, A. Abbott, und C. Schwartz. Sorting Nexin 3 (SNX3) Is Disrupted in a Patient With a Translocation T(6;13)(q21;q12) and Microcephaly, Microphthalmia, Ectrodactyly, Prognathism (MMEP) Phenotype. BMJ Group, 2002.

MLA Zitierstil

Vervoort, V., et al. Sorting Nexin 3 (SNX3) Is Disrupted in a Patient With a Translocation T(6;13)(q21;q12) and Microcephaly, Microphthalmia, Ectrodactyly, Prognathism (MMEP) Phenotype. BMJ Group, 2002.

Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.