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American Journal of Hematology|December 1, 1992
Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin KenyaJ S Waye, S P Cai, B Eng, et al.American Journal of Medical Genetics|August 15, 2001
Frequency and ethnic distribution of the common DHCR7 mutation in Smith-Lemli-Opitz syndromeM J Nowaczyk, L M Nakamura, B Eng, et al.Hemoglobin|November 1, 1994
Delta beta-thalassemia in an African-American: identification of the deletion endpoints and PCR-based diagnosisJ S Waye, B Eng, M B Coleman, et al.American Journal of Hematology|September 1, 1994
DNA diagnosis of Hb S and Hb Caribbean (alpha 2 beta 2 91 Leu-->Arg) in a Jamaican familyJ S Waye, M Patterson, B Eng, et al.Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 1, 1993
Carrier detection and prenatal diagnosis of hemoglobinopathies in OntarioJ S Waye, B Eng, S P Cai, et al.Blood|March 15, 1993
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemiaW Tang, S P Cai, B Eng, et al.American Journal of Hematology|September 18, 2001
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 casesJ S Waye, B Eng, M Patterson, et al.Hemoglobin|January 17, 2002
Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin geneJ S Waye, B Eng, M Patterson, et al.Blood|March 1, 1991
High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene regionJ S Waye, S P Cai, B Eng, et al.Annals of Neurology|July 18, 2001
Late-onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: compound heterozygosity for the IVS2+1G-->A mutation and a newly identified missense mutation (Thr408Ile) in a Spanish familyM Comabella, J S Waye, N Raguer, et al.Pageof 23