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American Journal of Human Genetics|November 19, 2019
Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male InfertilityPatrick Lorès, Denis Dacheux, Zine-Eddine Kherraf, et al.
American Journal of Human Genetics|November 19, 2019
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental AbnormalitiesLaura V Vandervore, Rachel Schot, Chiara Milanese, et al.
American Journal of Human Genetics|September 1, 1979
Linkage analysis and the inheritance of arches in a Habbanite isolateM W Anderson, B Bonné-Tamir, D Carmelli, et al.
American Journal of Human Genetics|December 5, 2017
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe AttachmentJohn R Shaffer, Jinxi Li, Myoung Keun Lee, et al.
American Journal of Human Genetics|December 5, 2017
Mutations in TUBB4B Cause a Distinctive Sensorineural DiseaseRomain Luscan, Sabrina Mechaussier, Antoine Paul, et al.
American Journal of Human Genetics|December 5, 2017
A Selection Operator for Summary Association Statistics Reveals Allelic Heterogeneity of Complex TraitsZheng Ning, Youngjo Lee, Peter K Joshi, et al.
American Journal of Human Genetics|January 15, 2019
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental DisorderRaphael Carapito, Ekaterina L Ivanova, Aurore Morlon, et al.
American Journal of Human Genetics|December 30, 2019
Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic HypogonadismAndrea Messina, Kristiina Pulli, Sara Santini, et al.
American Journal of Human Genetics|November 1, 1988
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.
American Journal of Human Genetics|February 27, 2018
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX ChildrenAnu Bashamboo, Caroline Eozenou, Anne Jorgensen, et al.
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