Stewart J. Payne

Molecular genetic analysis of the 3p- syndrome.

M E Phipps, J. Tolmie, M. Lerman, 1994, Human molecular genetics.

Stickler syndrome: Correlation between vitreoretinal phenotypes and linkage to COL 2A1

D. Barton, J. Yates, S. Payne, 1994, Eye.

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

A. Webster, A. Moore, F. Richards, 1996, Journal of medical genetics.

A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes.

K. Chotai, S. Payne, Stewart J. Payne, 1998, Journal of medical genetics.

Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families.

B. Ponder, C. Healey, D. Barton, 1994, Human molecular genetics.

Possible genotype-phenotype correlations in children with mild clinical course of Canavan disease.

D. Zafeiriou, H. Omran, J. Sass, 2005, Neuropediatrics.

Female germline mosaicism in tuberous sclerosis confirmed by molecular genetic analysis.

A. Green, T. Sepp, J. Yates, 1997, Human molecular genetics.