A. Evans

发表

Erratum: Detection of six novel FBN1 mutations in British patients affected by Marfan syndrome

A. Child, P. Comeglio, G. Brice, 2001, Human mutation.

Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema

A. Child, P. Comeglio, G. Brice, 2003, Journal of medical genetics.

Mapping of primary congenital lymphedema to the 5q35.3 region.

V. Sotirova, K. Burnand, A. Child, 1999, American journal of human genetics.

Leptin receptor gene variation and obesity: lack of association in a white British male population.

P. McKeigue, A. Strosberg, T. Aitman, 1997, Human molecular genetics.

Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats

J. Flint, T. Kurtz, T. Aitman, 1997, Nature Genetics.

A gene for lymphedema-distichiasis maps to 16q24.3.

A. Sigurdsson, M. Stratton, N. Rahman, 1999, American journal of human genetics.

Milroy disease and the VEGFR-3 mutation phenotype

K. Burnand, S. Mansour, A. Child, 2005, Journal of Medical Genetics.

The importance of mutation detection in Marfan syndrome and Marfan‐related disorders: report of 193 FBN1 mutations

Glen Brice, Gavin Arno, G. Arno, 2007, Human mutation.

Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus

A. Child, P. Comeglio, G. Brice, 2002, The British journal of ophthalmology.