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Annals of Human Genetics|June 17, 2017
Detection of Imprinting Effects for Quantitative Traits on X Chromosome Using Nuclear Families with Multiple DaughtersKexin Yu, Ji-Yuan Zhou, Wing Kam FungAnnals of Human Genetics|May 1, 1988
Assignment of complement components C4 binding protein (C4BP) and factor H (FH) to human chromosome 1q, using cDNA probesS Hing, A J Day, S J Linton, et al.Annals of Human Genetics|July 20, 2018
Analysis of causal effect of APOA5 variants on premature coronary artery diseaseFan Wang, Isabel Z Wang, Stephen Ellis, et al.Annals of Human Genetics|July 25, 2018
Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfectaMercedes Rodriguez Celin, Shahida Moosa, Virginia FanoAnnals of Human Genetics|July 12, 2018
CHRNA3 rs1051730 and CHRNA5 rs16969968 polymorphisms are associated with heavy smoking, lung cancer, and chronic obstructive pulmonary disease in a mexican populationRebeca Pérez-Morales, Alberto González-Zamora, María Fernanda González-Delgado, et al.Annals of Human Genetics|May 1, 1985
Differences in methylation on the active and inactive human X chromosomesS Lindsay, M Monk, R Holliday, et al.Annals of Human Genetics|October 21, 2009
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndromeChia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.Annals of Human Genetics|July 1, 1977
The linkage relationships of the haemoglobin beta, delta and alpha loci with 34 genetic marker systemsL R Weitkamp, G Stamatoyannopoulos, P T Rowley, et al.Annals of Human Genetics|July 1, 1977
Tracing quantitative measurements on human chromosomes in family studiesI J LauderAnnals of Human Genetics|July 1, 1977
Inbreeding effect on precocious mortality in Japanese communities of BrazilN Freire-Maia, N TakeharaPageof 231