Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?

MLA

Stange, Katja, et al. “Brachydactyly Type C Patient with Compound Heterozygosity for p.Gly319Val and p.Ile358Thr Variants in the GDF5 Proregion: Benign Variants or Mutations?” Journal of Human Genetics, vol. 60, no. 8, Aug. 2015, pp. 419–25. EBSCOhost, https://doi.org/10.1038/jhg.2015.48.

APA

Stange, K., Ott, C.-E., Schmidt-von Kegler, M., Gillesen-Kaesbach, G., Mundlos, S., Dathe, K., & Seemann, P. (2015). Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations? Journal of Human Genetics, 60(8), 419–425. https://doi.org/10.1038/jhg.2015.48

Chicago

Stange, Katja, Claus-Eric Ott, Mareen Schmidt-von Kegler, Gabriele Gillesen-Kaesbach, Stefan Mundlos, Katarina Dathe, and Petra Seemann. 2015. “Brachydactyly Type C Patient with Compound Heterozygosity for p.Gly319Val and p.Ile358Thr Variants in the GDF5 Proregion: Benign Variants or Mutations?” Journal of Human Genetics 60 (8): 419–25. doi:10.1038/jhg.2015.48.