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8. Genetic forms of hypopituitarism and their manifestation in the neonatal period. Alatzoglou KS, Dattani MT. Early Hum Dev; 2009 Nov; 85(11):705-12. PubMed ID: 19762173 [Abstract] [Full Text] [Related]
9. Mutations in PROP1 cause familial combined pituitary hormone deficiency. Wu W, Cogan JD, Pfäffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA, Rosenfeld MG. Nat Genet; 1998 Feb; 18(2):147-9. PubMed ID: 9462743 [Abstract] [Full Text] [Related]
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17. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia. Rainbow LA, Rees SA, Shaikh MG, Shaw NJ, Cole T, Barrett TG, Kirk JM. Clin Endocrinol (Oxf); 2005 Feb; 62(2):163-8. PubMed ID: 15670191 [Abstract] [Full Text] [Related]
18. Role of transcription factors in midline central nervous system and pituitary defects. Kelberman D, Dattani MT. Endocr Dev; 2009 Feb; 14():67-82. PubMed ID: 19293576 [Abstract] [Full Text] [Related]