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European Journal of Human Genetics : EJHG|July 21, 2001
Linear increase of diploidy in human sperm with age: a four-colour FISH studyM Bosch, O Rajmil, O Martínez-Pasarell, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
MUC1 gene polymorphism in the gastric carcinogenesis pathwayF Silva, F Carvalho, A Peixoto, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopiaN Matsumoto, R J Leventer, J A Kuc, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this regionAlison Male, Angela Davies, Anne Bergbaum, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Novel fibroblast growth factor receptor 3 (FGFR3) mutations in bladder cancer previously identified in non-lethal skeletal disordersBas W G van Rhijn, Angela A G van Tilborg, Irene Lurkin, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregateLouise M Downey, T Jeffrey Keen, Ismail K Jalili, et al.
European Journal of Human Genetics : EJHG|June 25, 2002
Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutationsMyrna Medlej-Hashim, Mirna Mustapha, Eliane Chouery, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorderEsther Leshinsky-Silver, Ami Zinger, Chaim N Bibi, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosisCéline Moutou, Nathalie Gardes, Stéphane Viville
European Journal of Human Genetics : EJHG|September 26, 2001
Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26M Mangino, E Flex, F Capon, et al.
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