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European Journal of Human Genetics : EJHG|November 28, 2000
Two novel mutations confirm FGD1 is responsible for the Aarskog syndromeC E Schwartz, G Gillessen-Kaesbach, M May, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndromeN Matsumoto, D E David, E W Johnson, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Simple two-color array-based approach for mutation detectionP Fortina, K Delgrosso, T Sakazume, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13R Cusano, S Gangarossa, P Forabosco, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populationsR Varon, E Seemanova, K Chrzanowska, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletionsR Paul, C Desnuelle, J Pouget, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Genetic structure of north-west Africa revealed by STR analysisE Bosch, F Calafell, A Pérez-Lezaun, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardationS Ranta, Y Zhang, B Ross, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Reproductive and menstrual history of females with fragile X expansionsA Murray, S Ennis, F MacSwiney, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
RNA-based mutation screening in German families with Sjögren-Larsson syndromeC Kraus, C Braun-Quentin, W G Ballhausen, et al.
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