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7 in total

1. Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development.

Authors: Nadean L Brown; Susan L Dagenais; Chuan-Min Chen; Tom Glaser
Journal: Mamm Genome Date: 2002-02 Impact factor: 2.957

2. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.

Authors: J Fang; S L Dagenais; R P Erickson; M F Arlt; M W Glynn; J L Gorski; L H Seaver; T W Glover
Journal: Am J Hum Genet Date: 2000-11-08 Impact factor: 11.025

Review 3. Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.

Authors: P de Bie; P Muller; C Wijmenga; L W J Klomp
Journal: J Med Genet Date: 2007-08-23 Impact factor: 6.318

Review 4. COMMD proteins: COMMing to the scene.

Authors: G N Maine; E Burstein
Journal: Cell Mol Life Sci Date: 2007-08 Impact factor: 9.261

5. New haplotypes in the Bedlington terrier indicate complexity in copper toxicosis.

Authors: Veronica A Coronado; Deepti Damaraju; Ritva Kohijoki; Diane W Cox
Journal: Mamm Genome Date: 2003-07 Impact factor: 2.957

Review 6. Canine models of copper toxicosis for understanding mammalian copper metabolism.

Authors: Hille Fieten; Peter A J Leegwater; Adrian L Watson; Jan Rothuizen
Journal: Mamm Genome Date: 2011-12-07 Impact factor: 2.957

7. Animal models of copper-associated liver disease.

Authors: I Carmen Fuentealba; Enrique M Aburto
Journal: Comp Hepatol Date: 2003-04-03

7 in total