Co-Occurrence of Hypertrophic Cardiomyopathy and Myeloproliferative Disorder in a Neonate with Noonan Syndrome Carrying Thr73Ile Mutation in PTPN11.

MLA

Yagasaki, Hideaki, et al. “Co-Occurrence of Hypertrophic Cardiomyopathy and Myeloproliferative Disorder in a Neonate with Noonan Syndrome Carrying Thr73Ile Mutation in PTPN11.” American Journal of Medical Genetics. Part A, vol. 167A, no. 12, Dec. 2015, pp. 3144–47. EBSCOhost, https://doi.org/10.1002/ajmg.a.37295.

APA

Yagasaki, H., Nakane, T., Hasebe, Y., Watanabe, A., Kise, H., Toda, T., Koizumi, K., Hoshiai, M., & Sugita, K. (2015). Co-Occurrence of Hypertrophic Cardiomyopathy and Myeloproliferative Disorder in a Neonate with Noonan Syndrome Carrying Thr73Ile Mutation in PTPN11. American Journal of Medical Genetics. Part A, 167A(12), 3144–3147. https://doi.org/10.1002/ajmg.a.37295

Chicago

Yagasaki, Hideaki, Takaya Nakane, Youhei Hasebe, Atsushi Watanabe, Hiroaki Kise, Takako Toda, Keiichi Koizumi, Minako Hoshiai, and Kanji Sugita. 2015. “Co-Occurrence of Hypertrophic Cardiomyopathy and Myeloproliferative Disorder in a Neonate with Noonan Syndrome Carrying Thr73Ile Mutation in PTPN11.” American Journal of Medical Genetics. Part A 167A (12): 3144–47. doi:10.1002/ajmg.a.37295.