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European Journal of Human Genetics : EJHG|October 22, 1998
A very high density microsatellite map (1 STR/41 kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical regionT C Cox, L L Cox, A BallabioGenesis (New York, N.Y. : 2000)|March 17, 2001
An X-linked GFP transgene reveals unexpected paternal X-chromosome activity in trophoblastic giant cells of the mouse placentaA K Hadjantonakis, L L Cox, P P Tam, et al.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 19, 2012
A landmark-free framework for the detection and description of shape differences in embryosS M Rolfe, L G Shapiro, T C Cox, et al.Human Molecular Genetics|October 13, 2000
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndromeT C Cox, L R Allen, L L Cox, et al.BMC Psychiatry|December 19, 2022
Evaluation of a workplace suicide prevention program in the Australian manufacturing industry: protocol for a cluster-randomised trial of MATES in manufacturingA D LaMontagne, L L Cox, C Lockwood, et al.Journal of Dental Research|August 3, 2017
Disrupted IRF6-NME1/2 Complexes as a Cause of Cleft Lip/PalateM T Parada-Sanchez, E Y Chu, L L Cox, et al.Journal of Dental Research|April 25, 2025
Splicing Defects and Cell Death Cause SF3B2-Linked Craniofacial MicrosomiaS Rao, K E N Watt, L Maili, et al.Pageof 1