P. Pearson

发表

The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YAC.

A. Monaco, D. Valle, H. Lehrach, 1993, Genomics.

Membrane fluidity measurements in peripheral cells from Huntington's disease patients

G. Beverstock, P. Pearson, 1981, Journal of neurology, neurosurgery, and psychiatry.

Fluorescent evidence for spermatocytes with two Y chromosomes in an XYY male

M. Hultén, P. Pearson, 1971, Annals of human genetics.

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

H. J. Evans, A. Bird, M. Jay, 1984, Nature.

Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only

S. McKee, J. Whittaker, R. B. van der Luijt, 2000, Journal of medical genetics.

Two different genes for X-linked retinitis pigmentosa.

B. Wirth, M. V. van Schooneveld, J. Donald, 1988, Genomics.

Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's disease

C. Wijmenga, R. Houwen, P. Pearson, 1998, European Journal of Human Genetics.

Electron spin resonance studies of erythrocyte ghost cells in Huntington's chorea

G. Beverstock, P. Pearson, 1982, Acta neurologica Scandinavica.

Frequency of Von Hippel‐Lindau germline mutations in classic and non‐classic Von Hippel‐Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation‐dependent probe amplification

P. Pearson, D. Halley, R. Sijmons, 2007, Clinical genetics.

The fragile X‐chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981–1986

G. Beverstock, J. Kamp, H. Veenema, 1988, Clinical genetics.

Germline mutations in the Von Hippel-Lindau ( VHL ) gene

D. Halley, B. Eussen, R. Luijt, 2000 .

Menkes kinky hair disease: A search for closely linked restriction fragment length polymorphism

H. Ropers, P. Wieacker, N. Horn, 2004, Human Genetics.

Managing all those bytes: the Human Genome Project.

A J Cuticchia, A. Cuticchia, M. Chipperfield, 1993, Science.

Mutation of the Duchenne muscular dystrophy gene associated with meiotic recombination

E. Bakker, P. Pearson, 1986, Clinical genetics.

Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3.

D. Valle, W. Kearns, N. Copeland, 1993, Genomics.

Localization of the polymorphic human calcitonin gene on chromosome 11

P. Pearson, E. Bakker, C. Lips, 2004, Human Genetics.

Genotype Assignment of Haemophilia A by Use of Intragenic and Extragenic Restriction Fragment Length Polymorphisms

P. Pearson, J. Dreesen, R. Quadt, 1987, Thrombosis and Haemostasis.