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4. Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion. Agarwal G; Bhatia V; Cook S; Thomas PQ J Clin Endocrinol Metab; 2000 Dec; 85(12):4556-61. PubMed ID: 11134108 [TBL] [Abstract][Full Text] [Related]
5. Cloning, characterization, and physical mapping of the canine Prop-1 gene (PROP1): exclusion as a candidate for combined pituitary hormone deficiency in German shepherd dogs. Lantinga-van Leeuwen IS; Kooistra HS; Mol JA; Renier C; Breen M; van Oost BA Cytogenet Cell Genet; 2000; 88(1-2):140-4. PubMed ID: 10773688 [TBL] [Abstract][Full Text] [Related]
6. Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. Pernasetti F; Toledo SP; Vasilyev VV; Hayashida CY; Cogan JD; Ferrari C; Lourenço DM; Mellon PL J Clin Endocrinol Metab; 2000 Jan; 85(1):390-7. PubMed ID: 10634415 [TBL] [Abstract][Full Text] [Related]
7. Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency. Fofanova O; Takamura N; Kinoshita E; Parks JS; Brown MR; Peterkova VA; Evgrafov OV; Goncharov NP; Bulatov AA; Dedov II; Yamashita S J Clin Endocrinol Metab; 1998 Jul; 83(7):2601-4. PubMed ID: 9661653 [TBL] [Abstract][Full Text] [Related]
8. Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency. Paracchini R; Giordano M; Corrias A; Mellone S; Matarazzo P; Bellone J; Momigliano-Richiardi P; Bona G Clin Genet; 2003 Aug; 64(2):142-7. PubMed ID: 12859410 [TBL] [Abstract][Full Text] [Related]
9. 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. de Graaff LC; Argente J; Veenma DC; Drent ML; Uitterlinden AG; Hokken-Koelega AC Horm Res Paediatr; 2010; 73(5):363-71. PubMed ID: 20389107 [TBL] [Abstract][Full Text] [Related]
10. A large deletion of PROP1 gene in patients with combined pituitary hormone deficiency from two unrelated Chinese pedigrees. Horm Res Paediatr; ; . PubMed ID: 20395664 [TBL] [Abstract][Full Text] [Related]