Congenital hypopituitarism due to POU1F1 gene mutation.

[1]  M. Dattani,et al.  Hypopituitarism Oddities: Congenital Causes , 2007, Hormone Research in Paediatrics.

[2]  V. Shotelersuk,et al.  A Novel Germline Mutation, IVS4+1G>A, of the POU1F1 Gene Underlying Combined Pituitary Hormone Deficiency , 2007, Hormone Research in Paediatrics.

[3]  M. Tullu,et al.  Kocher-debre-semelaigne syndrome with pericardial effusion , 2007 .

[4]  M. Dattani,et al.  Hypothalamic and pituitary development: novel insights into the aetiology. , 2007, European journal of endocrinology.

[5]  M. Dattani,et al.  Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. , 2005, The Journal of clinical endocrinology and metabolism.

[6]  T. Cole,et al.  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 , 2005, Clinical endocrinology.

[7]  S. Gallati,et al.  New N-terminal located mutation (Q4ter) within the POU1F1-gene (PIT-1) causes recessive combined pituitary hormone deficiency and variable phenotype. , 2003, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

[8]  M. Tullu,et al.  Kocher-Debre-Semelaigne syndrome: Hypothyroidism with muscle pseudohypertrophy , 2003, Indian journal of pediatrics.

[9]  D. Cowley,et al.  Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates , 2003, Clinical endocrinology.

[10]  G. Tell,et al.  Missense mutations of human homeoboxes: A review , 2001, Human mutation.

[11]  H. Eiken,et al.  Pituitary dwarfism in the R271W Pit-1 gene mutation , 1997, European Journal of Pediatrics.

[12]  J. Thijssen,et al.  Total deficiency of growth hormone and prolactin, and partial deficiency of thyroid stimulating hormone in two Dutch families: a new variant of hereditary pituitary deficiency. , 1989, Hormone research.

[13]  Ghosh Jb.  Kocher Debre Semelaigne syndrome in a neonate. , 1988 .

[14]  J. Ghosh.  Kocher Debre Semelaigne syndrome in a neonate. , 1988, Indian pediatrics.