M. Preece

发表

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues

P. Stanier, E. Wakeling, G. Moore, 1998, European Journal of Human Genetics.

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

J. Clayton-Smith, P. Stanier, D. Monk, 2002, Human Genetics.

Lack of Hemizygosity for the Insulin-Like Growth Factor I Receptor Gene in a Quantitative Study of 33 Silver Russell Syndrome Probands and Their Families

R. Trembath, P. Stanier, E. Wakeling, 1997, European journal of human genetics : EJHG.

Imprinted methylation profiles for proximal mouse Chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis

G. Kelsey, P. Stanier, D. Monk, 2003, Mammalian Genome.

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark.

Philip Stanier, Philippe Arnaud, David Monk, 2003, Human molecular genetics.

DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed

G. Kelsey, P. Stanier, D. Monk, 2002, Mammalian Genome.

Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.

S. Scherer, R. Weksberg, M. Meguro, 2002, Human molecular genetics.

Identification and characterization of an imprinted antisense RNA ( MESTIT 1 ) in the human MEST locus on chromosome 7 q 32

S. Scherer, R. Weksberg, M. Meguro, 2002 .

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

P. Stanier, M. Hitchins, G. Moore, 2001, Journal of medical genetics.

Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome

G. Bell, P. Stanier, D. Monk, 2001, European Journal of Human Genetics.

The Rubinstein‐Taybi syndrome: Occurrence in two sets of identical twins

M. Baraitser, M. Preece, 1983, Clinical genetics.

Phosphorylase kinase deﬁcient liver glycogenosis: progression to cirrhosis in infancy associated with PHKG2 mutations

P. Stanier, D. Monk, M. Hitchins, 2000 .

A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH‐binding activity by abolishing receptor homodimerization.

M. Preece, S. Amselem, M. Savage, 1994, The EMBO journal.

The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria

R. Trembath, M. Preece, S. Price, 1999, Journal of medical genetics.

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.

P Stanier, D Monk, E L Wakeling, 1999, American journal of human genetics.

An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands

P. Stanier, K. Abu-Amero, M. Preece, 1999, Journal of medical genetics.

Maternal uniparental disomy 7 in Silver-Russell syndrome.

R. Trembath, P. Stanier, M. Preece, 1997, Journal of medical genetics.

Final height and pubertal development in 55 children with idiopathic growth hormone deficiency, treated for between 2 and 15 years with human growth hormone

N. Cameron, N. Cameron, J. Tanner, 1981, European Journal of Pediatrics.

Growth hormone increases rate of pubertal maturation.

P. Hindmarsh, M. Preece, F. Darendeliler, 1990, Acta endocrinologica.

Physiological Growth Hormone Secretion and Response to Growth Hormone Treatment in Children with Short Stature and Intrauterine Growth Retardation

M. Preece, R. Stanhope, G. Hamill, 1989, Acta paediatrica Scandinavica. Supplement.

Increase in length of leg relative to trunk in Japanese children and adults from 1957 to 1977: comparison with British and with Japanese Americans.

J M Tanner, N Cameron, N. Cameron, 1982, Annals of human biology.

A longitudinal study of the growth in height of boys and girls of West Bengal (India) aged six months of 20 years.

J. Tanner, M. Preece, R. Hauspie, 1980, Annals of human biology.

Longitudinal study of leptin concentrations during puberty: sex differences and relationship to changes in body composition.

N. M. Drayer, D. Dunger, K. Ong, 1999, The Journal of clinical endocrinology and metabolism.

Prediction of adult height: methods and problems.

M. Preece, M. Preece, 1988, Acta paediatrica Scandinavica. Supplement.

British 1990 growth reference centiles for weight, height, body mass index and head circumference fitted by maximum penalized likelihood.

T J Cole, T. Cole, M. Preece, 1998, Statistics in medicine.

GROWTH HORMONE CELL ANTIBODIES AND PARTIAL GROWTH HORMONE DEFICIENCY IN A GIRL WITH TURNER'S SYNDROME

M. Preece, G. Bottazzo, C. McIntosh, 1980, Clinical endocrinology.

The genetic aetiology of Silver–Russell syndrome

P. Stanier, D. Monk, M. Preece, 2007, Journal of Medical Genetics.

Elevated leptin levels are associated with excess gains in fat mass in girls, but not boys, with type 1 diabetes: longitudinal study during adolescence.

D. Dunger, K. Ong, M. Preece, 2001, The Journal of clinical endocrinology and metabolism.

Growth reference charts for use in the United Kingdom

T. Cole, N. Cameron, M. Healy, 2002, Archives of disease in childhood.

Pulsatile growth hormone secretion in peripubertal patients with chronic renal failure. Cooperative Study Group on Pubertal Development in Chronic Renal Failure.

M. Preece, K. Schärer, F. Schaefer, 1991, The Journal of pediatrics.

Growth and endocrine function after renal transplantation.

M. Preece, G. Haycock, S. Greene, 1988, Archives of disease in childhood.

"Friendly fire" in medicine: hormones, homografts, and Creutzfeldt-Jakob disease

P. Brown, R. Will, M. Preece, 1992, The Lancet.

A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.

M. Preece, A. Green, S. Bundey, 1998, Journal of medical genetics.

Iatrogenic Creutzfeldt–Jakob disease at the millennium

L. McShane, I. Zerr, T. Sato, 2000, Neurology.

Long-term outcome of oxandrolone treatment in boys with constitutional delay of growth and puberty.

P. Hindmarsh, M. Preece, R. Stanhope, 1990, The Journal of pediatrics.

Laron‐type dwarfism with apparently normal high affinity serum growth hormone‐binding protein

M. Preece, H. Maheshwari, D. Morrell, 1991, Clinical endocrinology.

New height, weight and head circumference charts for British children with Williams syndrome

T J Cole, T. Cole, M. Preece, 2007, Archives of Disease in Childhood.

Relationship between insulin, insulin-like growth factor I, and dehydroepiandrosterone sulfate concentrations during childhood, puberty, and adult life.

D. Dunger, M. Preece, M. Savage, 1989, The Journal of clinical endocrinology and metabolism.

The effect of cyproterone acetate on the growth of children with central precocious puberty

M. Preece, R. Stanhope, D. Grant, 1987, European Journal of Pediatrics.

GROWTH HORMONE TREATMENT IN CHILDREN WITH CRANIOPHARYNGIOMA: FINAL GROWTH STATUS

N. Cameron, J. Tanner, M. Preece, 1981, Clinical endocrinology.

The genetic aetiology of Silver–Russell syndrome

P. Stanier, D. Monk, G. Moore, 2007, Journal of Medical Genetics.

FAMILIAL MALE PSEUDOHERMAPHRODITISM DUE TO DEFICIENCY OF 5α‐REDUCTASE

M. Preece, M. Savage, G. Rumsby, 1980 .

NOCTURNAL ADRENAL SUPPRESSION IN ASTHMATIC CHILDREN TAKING INHALED BECLOMETHASONE DIPROPIONATE

M. Preece, J. Honour, J. Warner, 1986, The Lancet.

Growth and development of male gymnasts, swimmers, soccer and tennis players: a longitudinal study.

N Maffulli, N. Maffulli, M. Preece, 1995, Annals of human biology.