William B. Rizzo

发表

Fatty aldehyde dehydrogenase: genomic structure, expression and mutation analysis in Sjögren-Larsson syndrome.

W. Rizzo, Z. Lin, G. Carney, 2001, Chemico-biological interactions.

Genomic organization, expression, and alternate splicing of the mouse fatty aldehyde dehydrogenase gene.

W. Rizzo, Z. Lin, G. Carney, 2000, Molecular genetics and metabolism.

The molecular basis of Sjögren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase gene.

W. Rizzo, Z. Lin, G. Carney, 1999, American journal of human genetics.

A common deletion mutation in European patients with Sjögren-Larsson syndrome.

V. de Laurenzi, V. Laurenzi, W. Rizzo, 1997, Biochemical and molecular medicine.

Sjögren-Larsson syndrome is caused by a common mutation in northern European and Swedish patients.

S. Bale, P. Steinert, V. de Laurenzi, 1997, The Journal of investigative dermatology.

Genetic homogeneity in Sjögren-Larsson syndrome: linkage to chromosome 17p in families of different non-Swedish ethnic origins.

S. Bale, W. Rizzo, A. Zlotogorski, 1995, American journal of human genetics.

Large contiguous gene deletions in Sjögren-Larsson syndrome.

W. Sanger, M. K. Rudd, O. Abdul-Rahman, 2011, Molecular genetics and metabolism.

Identification of new markers in Xp21 between DXS28 (C7) and DMD.

A. Ballabio, K. Worley, J. Towbin, 1992, Genomics.

Genomic organization and expression of the human fatty aldehyde dehydrogenase gene (FALDH).

V. de Laurenzi, W. Rizzo, J. Compton, 1997, Genomics.

Attitudes toward presymptomatic testing and prenatal diagnosis for adrenoleukodystrophy among affected families.

R. Abramson, R. Best, D. Costakos, 1991, American journal of medical genetics.