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Journal: Genes, 2022
Volume: 13
Number: 623
623
Article: Case Report: A Detailed Phenotypic Description of Patients and Relatives with Combined Central Hypothyroidism and Growth Hormone Deficiency Carrying IGSF1 Mutations
Authors: by Melitza S. M. Elizabeth, Anita Hokken-Koelega, Jenny A. Visser, Sjoerd D. Joustra and Laura C. G. de Graaff
Link: https://www.mdpi.com/2073-4425/13/4/623

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