J S Waye|B Eng - JoVE Visualize

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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.

Human Mutation|January 1, 1994

Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencingR D Hain, D Chitayat, R Cooper, et al.

Blood|March 1, 1992

Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin geneS P Cai, B Eng, W H Francombe, et al.

Pageof 12

Showing results (21-30 of 119) with videos related to

Sort By:

Pageof 12

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.

Human Mutation|January 1, 1994

Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencingR D Hain, D Chitayat, R Cooper, et al.

Blood|March 1, 1992

Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin geneS P Cai, B Eng, W H Francombe, et al.

Pageof 12