J. Crosby

发表

A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11.

D. Cox, J. Nadeau, E. Fuchs, 1989, Genomics.

Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation.

J. Nadeau, J. Crosby, D. Varnum, 1993, American journal of human genetics.

Mox-1 and Mox-2 define a novel homeobox gene subfamily and are differentially expressed during early mesodermal patterning in mouse embryos.

J. Nadeau, C. Wright, D. Noden, 1992, Development.

Zinc finger protein gene complexes on mouse chromosomes 8 and 11.

J. Nadeau, K. Chowdhury, C. Birkenmeier, 1990, Genomics.

Genetic maps of mouse chromosome 17 including 12 new anonymous DNA loci and 25 anchor loci.

M. Bucan, J. Nadeau, F. Michiels, 1991, Genomics.

Disorganization is a completely dominant gain-of-function mouse mutation causing sporadic developmental defects

J. Nadeau, J. Crosby, D. Varnum, 1992, Mechanisms of Development.

A complex of serine protease genes expressed preferentially in cytotoxic T-lymphocytes is closely linked to the T-cell receptor α- and δ-chain genes on mouse chromosome 14.

J. Nadeau, R. Bleackley, J. Crosby, 1990 .

The cardiac actin locus (Actc-1) is not on mouse chromosome 17 but is linked to beta 2-microglobulin on chromosome 2.

J. Nadeau, J. Crosby, S. J. Phillips, 1989, Genomics.

The murine retinoblastoma homolog maps to chromosome 14 near Es-10.

J. Nadeau, C. Kozak, J. Stone, 1989, Genomics.

Disorganization is a completely dominant gain-of-function mouse mutation causing sporadic developmental defects

J. Nadeau, J. Crosby, D. Varnum, 1992, Mechanisms of Development.