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European Journal of Human Genetics : EJHG|September 26, 2001
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genesA B West, A Zimprich, P J Lockhart, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genesA K Maiti, M G Mattéi, M Jorissen, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
mtDNA hypervariable region II (HVII) sequences in human evolution studiesA Salas, V Lareu, F Calafell, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Allelic association is increased by correlation of effective family sizeF Austerlitz, E Heyer
European Journal of Human Genetics : EJHG|August 31, 2001
N219Y, a new frequent mutation among mut(degree) forms of methylmalonic acidemia in Caucasian patientsC Acquaviva, J F Benoist, I Callebaut, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
Spectrum of mutations and genotype-phenotype analysis in Currarino syndromeJ Köchling, M Karbasiyan, A Reis
European Journal of Human Genetics : EJHG|August 31, 2001
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosisS Gerber, I Perrault, S Hanein, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
TP63 gene mutation in ADULT syndromeJ Amiel, G Bougeard, C Francannet, et al.
European Journal of Human Genetics : EJHG|July 12, 2002
Mutations of Cx26 gene (GJB2) for prelingual deafness in TaiwanYi-Chun Wang, Chiu-Yun Kung, Mao-Chang Su, et al.
European Journal of Human Genetics : EJHG|July 11, 2002
The 3'-untranslated region of the dystrophin gene - conservation and consequences of lossMarc J Greener, Caroline A Sewry, Francesco Muntoni, et al.
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