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Annals of Human Genetics|May 1, 1987
The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22M Azoulay, I Henry, F Tata, et al.Annals of Human Genetics|May 1, 1985
Heritable fragile sites on human chromosomes. XII. Population cytogeneticsG R SutherlandAnnals of Human Genetics|July 1, 1985
Further studies on bivalent chiasma frequency in human males with normal karyotypesD A Laurie, M A HulténAnnals of Human Genetics|July 1, 1985
Meiotic chromosome pairing in the normal human femaleB M Wallace, M A HulténAnnals of Human Genetics|October 1, 1985
Use of robust variance components models to analyse triglyceride data in familiesT H Beaty, S G Self, K Y Liang, et al.Annals of Human Genetics|November 8, 2012
Mutation detection in Croatian patients with familial hypercholesterolemiaIvan Pećin, Ros Whittall, Marta Futema, et al.Annals of Human Genetics|October 1, 1988
Confirmation of the relationship of HLA (chromosome 6) genes to depression and manic depression. II. The Ontario follow-up and analysis of 117 kindredsH C Stancer, L R Weitkamp, E Persad, et al.Annals of Human Genetics|October 1, 1988
A cytogenetic study of 47,XXY males of known origin and their parentsP A Jacobs, C Bacino, T Hassold, et al.Annals of Human Genetics|October 1, 1988
Effects of environmental changes on the phenotypic expression of human polygenic traitsL Ulizzi, R Correani, L TerrenatoAnnals of Human Genetics|August 7, 2020
The role of WNT1 mutant variant (WNT1c.677C>T ) in osteogenesis imperfectaBashan Zhang, Rong Li, Wenfeng Wang, et al.Pageof 231