2014
Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus
Bogardus H, Schulz VP, Maksimova Y, Miller BA, Li P, Forget BG, Gallagher PG. Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus. Haematologica 2014, 99: e168-e170. PMID: 24895341, PMCID: PMC4562552, DOI: 10.3324/haematol.2014.110312.Peer-Reviewed Original Research
1997
Comparison of SSCP analysis and CFLP analysis for mutation detection in the human iduronate 2‐sulfatase gene
Maddox L, Li P, Bennett A, Descartes M, Thompson J. Comparison of SSCP analysis and CFLP analysis for mutation detection in the human iduronate 2‐sulfatase gene. IUBMB Life 1997, 43: 1163-1171. PMID: 9442913, DOI: 10.1080/15216549700205001.Peer-Reviewed Original Research
1995
Mutations of the iduronate‐2‐sulfatase gene on a T146T background in three patients with Hunter syndrome
Li P, Huffman P, Thompson J. Mutations of the iduronate‐2‐sulfatase gene on a T146T background in three patients with Hunter syndrome. Human Mutation 1995, 5: 272-274. PMID: 7599640, DOI: 10.1002/humu.1380050314.Peer-Reviewed Original Research