Article Versions Notes

Elizabeth MSM, Hokken-Koelega A, Visser JA, Joustra SD, de Graaff LCG. Case Report: A Detailed Phenotypic Description of Patients and Relatives with Combined Central Hypothyroidism and Growth Hormone Deficiency Carrying IGSF1 Mutations. Genes. 2022; 13(4):623. https://doi.org/10.3390/genes13040623

Elizabeth, Melitza S. M., Anita Hokken-Koelega, Jenny A. Visser, Sjoerd D. Joustra, and Laura C. G. de Graaff. 2022. "Case Report: A Detailed Phenotypic Description of Patients and Relatives with Combined Central Hypothyroidism and Growth Hormone Deficiency Carrying IGSF1 Mutations" Genes 13, no. 4: 623. https://doi.org/10.3390/genes13040623

Elizabeth, M. S. M., Hokken-Koelega, A., Visser, J. A., Joustra, S. D., & de Graaff, L. C. G. (2022). Case Report: A Detailed Phenotypic Description of Patients and Relatives with Combined Central Hypothyroidism and Growth Hormone Deficiency Carrying IGSF1 Mutations. Genes, 13(4), 623. https://doi.org/10.3390/genes13040623