L. L. Barrow

Conserved linkage of neurotrophin-3 and von Willebrand factor on mouse Chromosome 6

K. Mohlke, M. Meisler, D. Ginsburg, 2004, Mammalian Genome.

Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts

J. Murray, H. van Bokhoven, R. Gorlin, 2002, Journal of medical genetics.

Aryl hydrocarbon receptor nuclear translocator 2 (ARNT2): structure, gene mapping, polymorphisms, and candidate evaluation for human orofacial clefts.

J. Murray, P. Romitti, M. Wines, 2002, Teratology.

SCNN1, an epithelial cell sodium channel gene in the conserved linkage group on mouse chromosome 6 and human chromosome 12.

M. Meisler, B. Rossier, C. Canessa, 1994, Genomics.

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.

D. G. Green, A. Boyle, M. Meisler, 1994, Genomics.

Conserved linkage of early growth response 4, annexin 4, and transforming growth factor alpha on mouse chromosome 6.

M. Meisler, K. Simin, D. C. Lee, 1994, Genomics.

Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6.

A. Swaroop, M. Meisler, W. Liu, 1994, Human molecular genetics.

Coeliac disease in twins

R. Gorlin, S. Daack-Hirsch, J. V. Bokhoven, 2002, Journal of medical genetics.