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A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35.

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Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop).

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An answer to a complex problem: cloning the mouse t-complex responder.

Mammalian genome : official journal of the International Mammalian Genome Society·2000

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death.

Proceedings of the National Academy of Sciences of the United States of America·2000

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X-linked gene for testicular feminization in the mouse

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X-chromosome inactivation and human genetic disease.

A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35.

Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop).

An answer to a complex problem: cloning the mouse t-complex responder.

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death.

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