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American Journal of Human Genetics|April 22, 2008
Estimating odds ratios in genome scans: an approximate conditional likelihood approachArpita Ghosh, Fei Zou, Fred A WrightAmerican Journal of Human Genetics|March 29, 2008
A Bayesian evaluation of human mitochondrial substitution ratesPhillip Endicott, Simon Y W HoAmerican Journal of Human Genetics|November 1, 1991
A maternal serum screen for trisomy 18: an extension of maternal serum screening for Down syndromeA J Staples, E F Robertson, E Ranieri, et al.American Journal of Human Genetics|May 20, 2008
Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndromeAlberto S Cornier, Karen Staehling-Hampton, Kym M Delventhal, et al.American Journal of Human Genetics|May 20, 2008
Two CES1 gene mutations lead to dysfunctional carboxylesterase 1 activity in man: clinical significance and molecular basisHao-Jie Zhu, Kennerly S Patrick, Hong-Jie Yuan, et al.American Journal of Human Genetics|March 18, 2014
Genetic origins of lactase persistence and the spread of pastoralism in AfricaAlessia Ranciaro, Michael C Campbell, Jibril B Hirbo, et al.American Journal of Human Genetics|April 1, 2014
De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disabilityDetelina Grozeva, Keren Carss, Olivera Spasic-Boskovic, et al.American Journal of Human Genetics|March 25, 2014
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhageDaniel Woo, Guido J Falcone, William J Devan, et al.American Journal of Human Genetics|April 8, 2014
Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear familiesMarc V Singleton, Stephen L Guthery, Karl V Voelkerding, et al.American Journal of Human Genetics|November 1, 1989
A cytogenetic investigation of the effects of cryopreservation on human spermJ E Chernos, R H MartinPageof 979