I. Rehman

发表

Loss of heterozygosity in sporadic primary cutaneous melanoma

E. Healy, J. Rees, B. Angus, 1995, Genes, chromosomes & cancer.

MULTIPLE SCLEROSIS PLAQUES REGIONAL DISTRIBUTION VARIATION IN CANADA AND PAKISTAN WITH REFERENCE TO GREY & WHITE MATTER: A RETROSPECTIVE ANALYSIS CARRIED OUT AT SERVICES HOSPITAL, LAHORE

I. Rehman, M. K. Khan, S. Abbas, 2018 .

Deletion mapping of chromosome 3p and 13q and preliminary analysis of the FHIT gene in human nonmelanoma skin cancer.

J. Rees, I. Rehman, S. Sikkink, 1997, The Journal of investigative dermatology.

Genetic change in actinic keratoses.

J. Rees, M. Takata, I. Rehman, 1996, Oncogene.

The temporal and spatial distribution of p21WAF expression in skin appendages

J. Rees, M. Takata, J. Rees, 2000, The British journal of dermatology.

Low frequency of allelic loss in skin tumours from immunosuppressed individuals.

J. Rees, M. Takata, A. Taylor, 1997, British Journal of Cancer.

A trichilemmal carcinoma arising from a proliferating trichilemmal cyst: the loss of the wild-type p53 is a critical event in malignant transformation.

J. Rees, M. Takata, I. Rehman, 1998, Human pathology.

Allelotypes of primary cutaneous melanoma and benign melanocytic nevi.

E. Healy, J. Rees, M. Takata, 1996, Cancer research.

Loss of heterozygosity analysis of keratoacanthoma reveals multiple differences from cutaneous squamous cell carcinoma.

J. Rees, M. Takata, I. Rehman, 1996, British Journal of Cancer.

Microsatellite instability in human non-melanoma and melanoma skin cancer.

E. Healy, J. Rees, A. Quinn, 1995, The Journal of investigative dermatology.

High frequency of loss of heterozygosity in actinic keratoses, a usually benign disease

E. Healy, J. Rees, A. Quinn, 1994, The Lancet.