J. Turton

发表

Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency.

M. Dattani, I. Robinson, P. Clayton, 2007, The Journal of clinical endocrinology and metabolism.

TCF7L1 is involved in hypothalamo-pituitary axis development in mice and humans

Stephen W. Wilson, S. A. Jayakody, J. Martinez-Barbera, 2016 .

1 TCF 7 L 1 is involved in hypothalamo-pituitary axis development in mice and humans

Stephen W. Wilson, S. A. Jayakody, J. Martinez-Barbera, 2016 .

Congenital hypopituitarism: clinical, molecular and neuroradiological correlates

M. Dattani, P. Hindmarsh, W. K. Chong, 2009, Clinical endocrinology.

Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency.

M. Dattani, P. Hindmarsh, P. Clayton, 2009, The Journal of clinical endocrinology and metabolism.

Transcription factor 7-like 1 is involved in hypothalamo–pituitary axis development in mice and humans

Stephen W. Wilson, S. A. Jayakody, M. Dattani, 2016, Proceedings of the National Academy of Sciences.

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism.

R. Lovell-Badge, M. Dattani, P. Thomas, 2005, American journal of human genetics.

Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.

M. Dattani, P. Clayton, J. Hamilton, 2005, The Journal of clinical endocrinology and metabolism.

The role of growth hormone in determining birth size and early postnatal growth, using congenital growth hormone deficiency (GHD) as a model

T. Cole, M. Dattani, P. Hindmarsh, 2005, Clinical endocrinology.

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)

M. Dattani, J. Starzyk, A. Tiulpakov, 2005, Clinical endocrinology.

HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.

M. Dattani, H. Krude, S. Shalet, 2007, The Journal of clinical endocrinology and metabolism.

Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD)

M. Dattani, S. Rhodes, P. Swift, 2009, Clinical endocrinology.

Genetic screening in a large cohort of patients with congenital hypopituitarism; current knowledge and future directions

M. Dattani, M. McCabe, E. Webb, 2012 .

Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation.

M. Dattani, S. Rhodes, M. McCabe, 2015, The Journal of clinical endocrinology and metabolism.

Two novel mutations in the POU1F1 gene generate null alleles through different mechanisms leading to combined pituitary hormone deficiency

M. Dattani, P. L. Le Tissier, P. Tissier, 2012, Clinical endocrinology.

Evolution of gonadotropin deficiency in a patient with type II autosomal dominant GH deficiency.

M. Dattani, I. Robinson, S. Aylwin, 2006, European journal of endocrinology.