Overgrowth Syndromes

Por Clayton-Smith, J
Publicado em 2002

Angelman's syndrome.

Por Clayton-Smith, J
Publicado em 1992

A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis.

Por Clayton-Smith, J, Donnai, D
Publicado em 1989

A further patient with the lethal type of Larsen syndrome.

Por Clayton-Smith, J, Donnai, D
Publicado em 1988

Fetal valproate syndrome.

Por Clayton-Smith, J, Donnai, D
Publicado em 1995

Cardiovascular malformations in Turner's syndrome.

Por Parchment, C, Clayton-Smith, J
Publicado em 1995

22q11 deletion: a cause of asymmetric crying facies.

Por Stewart, H S, Clayton-Smith, J
Publicado em 1996

Angelman syndrome: a review of the clinical and genetic aspects

Por Clayton-Smith, J, Laan, L
Publicado em 2003

Angelman syndrome.

Por Clayton-Smith, J, Pembrey, M E
Publicado em 1992

Evolving phenotype of Marfan's syndrome

Por Lipscomb, K., Clayton-Smith, J., Harris, R.
Publicado em 1997

Spontaneous aortic rupture in a 22-year-old.

Por Memon, M. A., Nicholson, C. M., Clayton-Smith, J.
Publicado em 1996

Letter To The Editor; Ocular coloboma and Fetal Valproate Syndrome: Four further cases and a hypothesis for aetiology

Por Jackson, A, Fryer, A, Clowes, V, Clayton-Smith, J
Publicado em 2014

Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.

Por Clayton-Smith, J, Webb, T, Cheng, X J, Pembrey, M E, Malcolm, S
Publicado em 1993

The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.

Por Donnai, D, Clayton-Smith, J, Gibbons, R J, Higgs, D R
Publicado em 1991

Examination of fetuses after induced abortion for fetal abnormality.

Por Clayton-Smith, J, Farndon, P A, McKeown, C, Donnai, D
Publicado em 1990

Dysmorphic features: an important clue to the diagnosis and severity of fetal anticonvulsant syndromes

Por Kini, U, Adab, N, Vinten, J, Fryer, A, Clayton‐Smith, J
Publicado em 2006

Dysmorphology at a distance: results of a web-based diagnostic service

Por Douzgou, S, Clayton-Smith, J, Gardner, S, Day, R, Griffiths, P, Strong, K
Publicado em 2014

Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM).

Por Black, G C, Perveen, R, Hatchwell, E, Reck, A, Clayton-Smith, J
Publicado em 1998

Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein

Por Watson, P., Black, G., Ramsden, S., Barrow, M., Super, M., Kerr, B., Clayton-Smith, J.
Publicado em 2001

Molecular mechanisms in Angelman syndrome: a survey of 93 patients.

Por Chan, C T, Clayton-Smith, J, Cheng, X J, Buxton, J, Webb, T, Pembrey, M E, Malcolm, S
Publicado em 1993