G. Adams

Cluster as the Molecular Basis for the Rare a-Thalassemia-1 (--/aa) in Blacks: HbH Disease in Sickle Cell Trait

Martin, Robert, H. Steinberg, 2005 .

De novo mutations in the 5′ regulatory region of the Norrie disease gene in retinopathy of prematurity

K. Gregory-Evans, C. Gregory‐Evans, P. Hykin, 2001, Journal of medical genetics.

Hyperkalaemic periodic paralysis in homozygous and heterozygous horses: a co-dominant genetic condition.

J. Naylor, C. Card, K. Lightfoot, 1999, Equine Veterinary Journal.

Ethnic divergence and linkage disequilibrium of novel SNPs in the human NLI-IF gene: evidence of human origin and lack of association with tuberculosis susceptibility

E. Graviss, L. Teeter, Xin Ma, 2002, Journal of Human Genetics.

Recurrent heterozygous PAX6 missense variants cause severe bilateral microphthalmia via predictable effects on DNA–protein interaction

E. Tobias, P. Calvas, J. Marsh, 2019 .