P. S. Hart

Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome

D. Bowden, Yingze Zhang, T. Hart, 1999, Journal of medical genetics.

Polymorphism (g2035C>T) in the amelogenin gene

T. Hart, P. S. Hart, J.T. Wright, 2000, Human mutation.

Hereditary persistence of alpha-fetoprotein in a child with testicular germ cell tumor.

P. Cochran, S. D. de Graaf, A. Chauvenet, 1999, Medical and pediatric oncology.

Salivary abnormalities in Prader-Willi syndrome.

P. S. Hart, 1994, Annals of the New York Academy of Sciences.

Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicism

P. N. Rao, M. Pettenati, J. Rosnes, 1999, Prenatal Diagnosis.

Improved method of isolation of DNA from celloidin‐embedded tissue

P. S. Hart, Robert I. Kohut, A. Charla Vlaservich, 1999, The Laryngoscope.

Harnessing Information Using Genomic Platforms

W. Gahl, T. Markello, P. Hart, 2012 .

An integrated physical and genetic map of the PLS locus interval on Chromosome 11q14

S. Walker, D. Bowden, T. Hart, 2000, Mammalian Genome.