Amino acid sequence of human prothrombin fragments 1 and 2.

Por Walz, D A, Hewett-Emmett, D, Seegers, W H
Publicado em 1977

Rapid evolution of the human gene for cytochrome c oxidase subunit IV.

Por Lomax, M I, Hewett-Emmett, D, Yang, T L, Grossman, L I
Publicado em 1992

Nucleotide sequence of human liver carbonic anhydrase II cDNA.

Por Montgomery, J C, Venta, P J, Tashian, R E, Hewett-Emmett, D
Publicado em 1987

Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.

Por Sly, W S, Hewett-Emmett, D, Whyte, M P, Yu, Y S, Tashian, R E
Publicado em 1983

Weak male-driven molecular evolution in rodents.

Por Chang, B H, Shimmin, L C, Shyue, S K, Hewett-Emmett, D, Li, W H
Publicado em 1994

High polymorphism at the human melanocortin 1 receptor locus.

Por Rana, B K, Hewett-Emmett, D, Jin, L, Chang, B H, Sambuughin, N, Lin, M, Watkins, S, Bamshad, M, Jorde, L B, Ramsay, M, Jenkins, T, Li, W H
Publicado em 1999