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European Journal of Human Genetics : EJHG|December 8, 2005
Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1Ahmed Bouhouche, Ali Benomar, Naima Bouslam, et al.European Journal of Human Genetics : EJHG|December 8, 2005
A novel mutation in PAX9 causes familial form of molar oligodontiaAdrianna Mostowska, Barbara Biedziak, Wieslaw H TrzeciakEuropean Journal of Human Genetics : EJHG|November 25, 2005
Optimal genotype determination in highly multiplexed SNP dataMartin Moorhead, Paul Hardenbol, Farooq Siddiqui, et al.European Journal of Human Genetics : EJHG|January 1, 1993
Striking founder effect for the fragile X syndrome in FinlandC Oudet, H von Koskull, A M Nordström, et al.European Journal of Human Genetics : EJHG|January 1, 1993
A five-year prospective study of the health of children in different ethnic groups, with particular reference to the effect of inbreedingS Bundey, H AlamEuropean Journal of Human Genetics : EJHG|January 1, 1994
The 8993 mtDNA mutation: heteroplasmy and clinical presentation in three familiesY Tatuch, R A Pagon, B Vlcek, et al.European Journal of Human Genetics : EJHG|January 14, 2010
Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population samplePenelope A Lind, Michelle Luciano, Margaret J Wright, et al.European Journal of Human Genetics : EJHG|July 6, 2000
Complex patterns of male germline instability and somatic mosaicism in myotonic dystrophy type 1L Martorell, D G Monckton, J Gamez, et al.European Journal of Human Genetics : EJHG|July 6, 2000
An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian familyA Baumer, S Belli, R M Trüeb, et al.European Journal of Human Genetics : EJHG|July 6, 2000
Combined segregation and linkage analysis of 59 Hodgkin's disease families indicates the role of HLA determinantsY Y Shugart, A CollinsPageof 563