E. Mateu

发表

Allele frequencies for 20 microsatellites in a worldwide population survey.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1997, Human heredity.

Sequence variability of a human pseudogene.

A. Andrés, D. Comas, J. Bertranpetit, 2001, Genome research.

[Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations].

F. Prieto, M. Beneyto, E. Mateu, 2001, Medicina clinica.

Population Genetics of Y-Chromosome Short Tandem Repeats in Humans

Francesc Calafell, Jaume Bertranpetit, David Comas, 1997, Journal of Molecular Evolution.

A tale of two islands: population history and mitochondrial DNA sequence variation of Bioko and São Tomé, Gulf of Guinea

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1997, Annals of Human Genetics.

Worldwide genetic analysis of the CFTR region.

K. Kidd, J. Kidd, A. Pakstis, 2001, American journal of human genetics.

Trading genes along the silk road: mtDNA sequences and the origin of central Asian populations.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1998, American journal of human genetics.

Profiles of accepted mutation: from neutrality in a pseudogene to disease-causing mutation on its homologous gene

J. Bertranpetit, R. Martínez-Arias, F. Calafell, 2001, Human Genetics.

Allele frequencies of 13 short tandem repeats in population samples from the Iberian Peninsula and Northern Africa

A. Pérez-Lezaun, J. Bertranpetit, J. Clarimón, 2000, International Journal of Legal Medicine.

HLA evidence for the lack of genetic heterogeneity in Basques

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1998, Annals of human genetics.

HLA class I and class II DNA typing and the origin of Basques.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1998, Tissue antigens.

Can a place of origin of the main cystic fibrosis mutations be identified?

J. Bertranpetit, T. Casals, F. Calafell, 2002, American journal of human genetics.

Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR Gene

K. Kidd, J. Kidd, J. Bertranpetit, 1999, Human Heredity.

Sex-specific migration patterns in Central Asian populations, revealed by analysis of Y-chromosome short tandem repeats and mtDNA.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1999, American journal of human genetics.

A constitutional homozygous mutation in theRB1 gene in a patient with unilateral retinoblastoma

F. Prieto, M. Beneyto, E. Mateu, 2000, Journal of medical genetics.

Paternal and maternal lineages in the Balkans show a homogeneous landscape over linguistic barriers, except for the isolated Aromuns

D. Comas, A. González-Neira, F. Calafell, 2005, Annals of human genetics.

Genetics of retinoblastoma: a study.

F. Prieto, M. Hernández, M. Beneyto, 1997, Cancer genetics and cytogenetics.

Genetic structure of north-west Africa revealed by STR analysis

A. Pérez-Lezaun, D. Comas, A. Cambon-Thomsen, 2000, European Journal of Human Genetics.

Spatial patterns of cystic fibrosis mutation spectra in European populations

A. Andrés, J. Bertranpetit, O. Lao, 2003, European Journal of Human Genetics.

Population history of north Africa: evidence from classical genetic markers.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1997, Human biology.

Microsatellite variation and the differentiation of modern humans

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1996, Human Genetics.

Glucocerebrosidase pseudogene variation and Gaucher disease: Recognizing pseudogene tracts in GBA alleles

D. Comas, J. Bertranpetit, R. Martínez-Arias, 2001, Human mutation.

Geographic variation in human mitochondrial DNA control region sequence: the population history of Turkey and its relationship to the European populations.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1996, Molecular biology and evolution.

PKLR-GBA region shows almost complete linkage disequilibrium over 70 kb in a set of worldwide populations

A. Andrés, A. Pérez-Lezaun, J. Bertranpetit, 2002, Human Genetics.

Mitochondrial DNA variation and the origin of the Europeans

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1997, Human Genetics.