APA

Zhao Z., Jiang Y., Li B., Yang F., Li J., Jin X., Ning S. & Sun S. (20171129). Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient. : BMC medical genetics.

Chicago

Zhao Zi-Ye, Jiang Yu-Liang, Li Bai-Rong, Yang Fu, Li Jing, Jin Xiao-Wei, Ning Shou-Bin and Sun Shu-Han. 20171129. Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient. : BMC medical genetics.

Harvard

Zhao Z., Jiang Y., Li B., Yang F., Li J., Jin X., Ning S. and Sun S. (20171129). Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient. : BMC medical genetics.

MLA

Zhao Zi-Ye, Jiang Yu-Liang, Li Bai-Rong, Yang Fu, Li Jing, Jin Xiao-Wei, Ning Shou-Bin and Sun Shu-Han. Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient. : BMC medical genetics. 20171129.