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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Query Trace: Familial Hypopituitarism[original query]
HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
The Journal of clinical endocrinology and metabolism 2007 Feb 92 (2): 691-7.
McNay David E G, Turton James P, Kelberman Daniel, Woods Kathryn S, Brauner Raja, Papadimitriou Anastasios, Keller Eberhard, Keller Alexandra, Haufs Nele, Krude Heiko, Shalet Stephen M, Dattani Mehul
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