Cite
Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant.
MLA
Huby, Thomas, et al. “Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant.” Journal of Clinical Endocrinology & Metabolism, vol. 107, no. 4, Apr. 2022, pp. 1367–73. EBSCOhost, https://doi.org/10.1210/clinem/dgab894.
APA
Huby, T., Guillou, E. L., des Roziers, C. B., Pacot, L., Briand-Suleau, A., Chansavang, A., Toussaint, A., Duchossoy, V., Vaucouleur, N., Benoit, V., Lodé, L., Molac, C., North, M.-O., Grotto, S., Tsatsaris, V., Jouinot, A., Cochand-Priollet, B., Paepegaey, A.-C., Nectoux, J., & Groussin, L. (2022). Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant. Journal of Clinical Endocrinology & Metabolism, 107(4), 1367–1373. https://doi.org/10.1210/clinem/dgab894
Chicago
Huby, Thomas, Edouard Le Guillou, Cyril Burin des Roziers, Laurence Pacot, Audrey Briand-Suleau, Albain Chansavang, Aurélie Toussaint, et al. 2022. “Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant.” Journal of Clinical Endocrinology & Metabolism 107 (4): 1367–73. doi:10.1210/clinem/dgab894.