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1 growth pathogenesis associated with combined pituitary hormone deficiency.
2 ses, giving rise to the syndrome of combined pituitary hormone deficiency.
3 fied in several human families with multiple pituitary hormone deficiencies.
5 n patients with retarded growth and combined pituitary hormone deficiency and also abnormal neck and
7 complex diseases featuring combined anterior pituitary hormone deficiency and, in specific cases, los
8 isolated growth hormone deficiency, combined pituitary hormone deficiency, and syndromes such as sept
9 ne deficiency, either alone or with multiple pituitary hormone deficiencies, as identified by clinica
11 2 regions have been associated with combined pituitary hormone deficiency (CPHD) diseases, suggesting
15 x transcription factors LHX4 and PROP1 cause pituitary hormone deficiency in both humans and mice.
16 ons in the gene are associated with combined pituitary hormone deficiency in human patients and anima
18 e show here that this novel form of combined pituitary hormone deficiency is characterized by the per
19 ation in human PIT1(R271W), causing combined pituitary hormone deficiency, results in loss of Pit1 as
20 th fronto-temporal lobe hypoplasia, multiple pituitary hormone deficiency, seizures, severe visual im
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