S. P. Covello

The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.

H. Kremer, J. Uitto, J. McGrath, 1999, American journal of human genetics.

A new gene for pachyonychia congenita type 2: Keratin K6B is the expression partner of K17 in epidermal appendages

J. Uitto, H. Goor, W. McLean, 1998 .

A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2.

J. Uitto, C. Coleman, F. Smith, 1998, Human molecular genetics.

Genomic organization and fine mapping of the keratin 2e gene (KRT2E): K2e V1 domain polymorphism and novel mutations in ichthyosis bullosa of Siemens.

E. Lane, J. Uitto, I. Leigh, 1998, The Journal of investigative dermatology.

Identification of novel glucocorticoid-response elements in human elastin promoter and demonstration of nucleotide sequence specificity of the receptor binding.

J. Uitto, G. Litwack, S. P. Covello, 1997, The Journal of investigative dermatology.

A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy.

J. Uitto, C. Coleman, S. Hannush, 1999, American journal of ophthalmology.

A case of extraskeletal osteosarcoma with metastasis to the skin.

Jason B. Lee, Jason B Lee, T. Humphreys, 2003, Journal of the American Academy of Dermatology.

Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2

Munro, C. S. Coleman, R. Tenconi, 1998, The British journal of dermatology.