Case Report: A Novel Point Mutation of SOX3 in a Subject With Growth Hormone Deficiency, Hypogonadotrophic Hypogonadism, and Borderline Intellectual Disability

Overview of attention for article published in Frontiers in endocrinology, February 2022

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Case Report: A Novel Point Mutation of SOX3 in a Subject With Growth Hormone Deficiency, Hypogonadotrophic Hypogonadism, and Borderline Intellectual Disability https://t.co/2ffoZKvIoW

20 Mar 2022

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RT @FrontEndocrinol: New Research: Case Report: A Novel Point Mutation of SOX3 in a Subject With Growth Hormone Deficiency, Hypogonadotroph…

28 Feb 2022

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New Research: Case Report: A Novel Point Mutation of SOX3 in a Subject With Growth Hormone Deficiency, Hypogonadotrophic Hypogonadism, and Borderline Intellectual Disability: SOX3 is critical for the development of the pituitary,… https://t.co/P57zfy7ySy #

28 Feb 2022

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