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European Journal of Human Genetics : EJHG|September 26, 2001
Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenariansG Rose, G Passarino, G Carrieri, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
Mitochondrial DNA characterisation of European isolates: the Maragatos from SpainJ M Larruga, F Díez, F M Pinto, et al.
European Journal of Human Genetics : EJHG|April 24, 2003
Chromosome instability and nibrin protein variants in NBS heterozygotesCaterina Tanzanella, Antonio Antoccia, Emanuela Spadoni, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
Overgrowth syndromes: is dysfunctional PI3-kinase signalling a unifying mechanism?Karen T Barker, Richard S Houlston
European Journal of Human Genetics : EJHG|August 2, 2003
Computer-based recognition of dysmorphic facesHartmut S Loos, Dagmar Wieczorek, Rolf P Würtz, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
Indication of linkage and genetic heterogeneity for asthma and atopy on chromosomes 8p and 12q in 107 French EGEA familiesM-H Dizier, H Quesneville, C Besse-Schmittler, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
Manic depressive illness in a founder populationEvelyne Heyer, Bruno Toupance, Cesare Perri, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1Muhammad Arshad Rafique, Muhammad Ansar, Syed Muhammad Jamal, et al.
European Journal of Human Genetics : EJHG|August 2, 2003
SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6C H Zühlke, M Spranger, S Spranger, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysisVoula Velissariou, Thalia Antoniadi, Jolanda Gyftodimou, et al.
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