P L Pearson

发表

Report of the Committee on Comparative Mapping: Conference on Human Gene Mapping 4.

P L Pearson, T H Roderick, T. Roderick, 1978 .

The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromes.

P L Pearson, A M Zwamborn-Hanssen, J B Bijlsma, 1997, American journal of medical genetics.

LEYTAS: a system for the processing of microscopic images.

J S Ploem, P L Pearson, J Vrolijk, 1980, Analytical and quantitative cytology.

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.

P L Pearson, R. Sinke, P. Wesseling, 2004, Brain : a journal of neurology.

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

P L Pearson, J. Buitelaar, R. Sinke, 2003, American journal of human genetics.

The GDB Human Genome Data Base Anno 1992.

N W Matheson, P L Pearson, R J Robbins, 1992, Nucleic acids research.

Towards an understanding of the genetics of human male infertility: lessons from flies.

P L Pearson, R. Hochstenbach, P. Pearson, 2000, Trends in genetics : TIG.

Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q.

P L Pearson, J Hermans, P. Devilee, 1991, Oncogene.

The human genome initiative--do databases reflect current progress?

P L Pearson, B. Maidak, P. Pearson, 1991, Science.

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family

P L Pearson, B P C van de Warrenburg, R. Sinke, 2003, Neurology.