M Claustres

A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases

R G H Cotton, A D Auerbach, A F Brown, 2007, Human mutation.

Linkage disequilibrium between the M470V variant and the IVS8 polyT alleles of the CFTR gene in CBAVD.

M Claustres, M. Claustres, J. Demaille, 1998, Journal of medical genetics.

Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study.

M Claustres, C Binquet, E. Arbustini, 2007, American journal of human genetics.

[Detection of deletions by the amplification of exons (multiplex PCR) in Duchenne muscular dystrophy].

M Claustres, M Desgeorges, C Boileau, 1989, Journal de genetique humaine.

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.

M Claustres, W Lissens, X. Estivill, 1995, The New England journal of medicine.