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Cell|January 16, 2007
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humansDavid A Keays, Guoling Tian, Karine Poirier, et al.American Journal of Medical Genetics|July 14, 1999
Follow-up study on a susceptibility locus for schizophrenia on chromosome 6qM Martinez, L R Goldin, Q Cao, et al.Proceedings of the National Academy of Sciences of the United States of America|August 20, 2005
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screenDebora Bogani, Catherine Willoughby, Jennifer Davies, et al.Nature Genetics|July 2, 2003
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31Philomena Mburu, Mirna Mustapha, Anabel Varela, et al.Plos One|February 6, 2013
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5Nellie Y Loh, Liz Bentley, Henrik Dimke, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 30, 2021
INFRAFRONTIER quality principles in systemic phenotypingHilke Ehlich, Heather L Cater, Ann M Flenniken, et al.Physiological Genomics|May 29, 2008
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory studySilvia Mandillo, Valter Tucci, Sabine M Hölter, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 7, 2002
Novel phenotypes identified by plasma biochemical screening in the mouseTertius A Hough, Patrick M Nolan, Vicky Tsipouri, et al.Nature|November 23, 2018
Helios is a key transcriptional regulator of outer hair cell maturationLauren Chessum, Maggie S Matern, Michael C Kelly, et al.Genome Research|July 13, 1999
A high-density integrated genetic linkage and radiation hybrid map of the laboratory ratR G Steen, A E Kwitek-Black, C Glenn, et al.Pageof 48