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Annals of Human Genetics|January 11, 2005
The contribution of genetic and environmental factors to quantitative variability of erythrocyte membrane proteins in primary hypotensionV P Ivanov, A V Polonikov, M A SolodilovaAnnals of Human Genetics|January 11, 2005
beta2-Adrenergic receptor gene variations associated with stage-2 hypertension in northern Han ChineseD Ge, J Huang, J He, et al.Annals of Human Genetics|January 11, 2005
Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroupsElena B Starikovskaya, Rem I Sukernik, Olga A Derbeneva, et al.Annals of Human Genetics|February 22, 2005
SNP haplotypes in the angiotensin I-converting enzyme (ACE) gene: analysis of Nigerian family data using gamete competition modelsC A McKenzie, J S Sinsheimer, A A Adeyemo, et al.Annals of Human Genetics|January 1, 1987
Characterization and use of somatic cell hybrids with interspecific translocations involving the human X chromosomeY BoydAnnals of Human Genetics|January 11, 2022
A large-scale genetic correlation scan between rheumatoid arthritis and human blood metabolitesGuolian Yuan, Pan Luo, Ke Xu, et al.Annals of Human Genetics|July 1, 1986
Genetic polymorphism of esterase B3 in human leukocytesP M Coates, J A CortnerAnnals of Human Genetics|July 1, 1987
The gene for human alpha-lactalbumin is assigned to chromosome 12q13M S Davies, L F West, M B Davis, et al.Annals of Human Genetics|December 10, 2021
CFTR mutational screening by next-generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern populationChantal Farra, Johnny Awwad, Lama Hamadeh, et al.Annals of Human Genetics|August 30, 2022
A splice site variant in TCTN3 underlies an atypical form of orofaciodigital syndrome IVShabir Hussain, Shoaib Nawaz, Hammal Khan, et al.Pageof 231