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Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency
Author(s):
I. Netchine
,
ML Sobrier
,
H Krude
,
D Schnabel
,
M. Maghnie
,
E Marcos
Publication date:
2000
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Journal of the ASEAN Federation of Endocrine Societies
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ScienceOpen disciplines:
Endocrinology & Diabetes
,
Medicine
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