Teresa Webb
(Former)
1 - 9 out of 9Page size: 10
Publications
- 2019
- Published
Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection
& 217 others, , 2019, In: Journal of the American College of Cardiology.Research output: Contribution to journal › Article › peer-review
- 2014
- Published
A longitudinal follow-up study of people with Prader–Willi syndrome with psychosis and those at increased risk of developing psychosis due to genetic subtype
Teresa Webb, 1 Aug 2014, In: Psychological Medicine. 44, 11, p. 2431-2435Research output: Contribution to journal › Article › peer-review
- 2003
- Published
Developmental delay and the methyl binding genes
Farida Latif & Teresa Webb, 1 Feb 2003, In: Journal of Medical Genetics. 40, 2, p. e13Research output: Contribution to journal › Article
- 2002
- Published
Prader-Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey
Teresa Webb, 1 Apr 2002, In: British Journal of Psychiatry. 180, p. 358-362 5 p.Research output: Contribution to journal › Article
- Published
Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study
Teresa Webb, 1 Apr 2002, In: Developmental Medicine and Child Neurology. 44, 4, p. 248-255 8 p.Research output: Contribution to journal › Article
- 2001
- Published
Population prevalence and estimated birth incidence and mortality rate of people with Prader-Willi syndrome in one UK health region
Teresa Webb, 1 Nov 2001, In: Journal of Medical Genetics. 38, 11, p. 792-798 7 p.Research output: Contribution to journal › Article
- Published
Guidelines for reportive clinical features in cases with MECP2 mutations
Teresa Webb, 1 Jul 2001, In: Brain and Development. 23, 4, p. 208-211 4 p.Research output: Contribution to journal › Article
- Published
Rett Syndrome and the MECP2 gene
Teresa Webb & Farida Latif, 1 Apr 2001, In: Journal of Medical Genetics. 38, 4, p. 217-223 7 p.Research output: Contribution to journal › Article
- 2000
- Published
Mutations in the MECP2 gene in a cohort of girls with Rett syndrome
Farida Latif & Teresa Webb, 1 Aug 2000, In: Journal of Medical Genetics. 37, 8, p. 610-612 3 p.Research output: Contribution to journal › Article