PROP1, HESX1, POU1F1, LHX3 and LHX4 Mutation and Deletion Screening and GH1 P89L and IVS3+1/+2 Mutation Screening in a Dutch Nationwide Cohort of Patients with Combined Pituitary Hormone Deficiency

Publisher： Karger

E-ISSN： 1663-2826|73|5|363-371

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.73, Iss.5, 2010-04, pp. : 363-371

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