Xavier Estivill

Molecular cloning, expression, and chromosomal localization of a ubiquitously expressed human 6-phosphofructo-2-kinase/ fructose-2,6-bisphosphatase gene (PFKFB3)

X. Estivill, J. L. Rosa, F. Ventura, 1999, Cytogenetic and Genome Research.

Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1.

X. Estivill, M. Gallucci, P. Gasparini, 1997, American journal of human genetics.

Cloning and characterization of human FTCD on 21q22.3, a candidate gene for glutamate formiminotransferase deficiency

X. Estivill, S. de la Luna, A. Solans, 2000, Cytogenetic and Genome Research.

Dating the Origin of the CCR 5D 32 AIDS-Resistance Allele by the Coalescence of Haplotypes

H. Ostrer, D. Goldstein, X. Estivill, 2007 .

Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation

X. Estivill, P. Gasparini, M. Carella, 2005, Journal of Medical Genetics.

Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

X. Estivill, N. López-Bigas, P. Gasparini, 2002, Human mutation.