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Annals of Human Genetics|September 1, 1996
Identification of an E689K substitution as the molecular basis of the human acid alpha-glucosidase type 4 allozyme (GAA*4)M L Huie, M Menaker, P J McAlpine, et al.Annals of Human Genetics|September 1, 1996
Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' diseaseI P Tomlinson, S Olschwang, D Abelovitch, et al.Annals of Human Genetics|January 1, 1996
Chromosomal localisation of genes coding for human and mouse liver cytosolic cysteine dioxygenaseS Jeremiah, K P McCann, A C Williams, et al.Annals of Human Genetics|January 1, 1996
From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and TurksF Calafell, P Underhill, A Tolun, et al.Annals of Human Genetics|January 1, 1996
Ethnicity and myotonic dystrophy: a possible explanation for its absence in sub-Saharan AfricaA Goldman, M Ramsay, T JenkinsAnnals of Human Genetics|January 1, 1996
Racial heterogeneity of DNA polymorphisms linked to the A and the O alleles of the ABO blood group geneM A Zago, M H Tavella, B P Simões, et al.Annals of Human Genetics|March 1, 1996
Mitotic recombination among acrocentric chromosomes' short armsU Guissani, B Facchinetti, G Cassina, et al.Annals of Human Genetics|March 1, 1996
Determining approximate estimates of inheritance parameters from sib-pair IBD proportionsJ R Green, S ShahAnnals of Human Genetics|April 1, 2008
Quantification of the genetic component of basal C-reactive protein expression in SLE nuclear familiesB Rhodes, J Meek, J C Whittaker, et al.Annals of Human Genetics|June 3, 2008
Using population mixtures to optimize the utility of genomic databases: linkage disequilibrium and association study design in IndiaT J Pemberton, M Jakobsson, D F Conrad, et al.Pageof 231