Martin, D., Probst, F., Camper, S., & Petty, E. (2000). Characterisation and genetic mapping of a new X linked deafness syndrome. BMJ Group.
Citação norma ChicagoMartin, D., F. Probst, S. Camper, and E. Petty. Characterisation and Genetic Mapping of a New X Linked Deafness Syndrome. BMJ Group, 2000.
MLA引文Martin, D., F. Probst, S. Camper, and E. Petty. Characterisation and Genetic Mapping of a New X Linked Deafness Syndrome. BMJ Group, 2000.
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