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J S Waye

Showing results (71-80 of 115) with videos related to

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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.
British Journal of Haematology|October 7, 2000
Compound heterozygosity for triplicated alpha-globin gene and (- -(SEA)) alpha-globin gene deletion: implication for thalassaemia screeningS K Ma, A Y Chan, L C CHan, et al.
American Journal of Hematology|February 3, 1999
A novel and de novo spontaneous point mutation (Glu271STOP) of the antithrombin gene results in a type I deficiency and thrombophiliaM D Tarantino, S M Curtis, G S Johnson, et al.
British Journal of Haematology|September 1, 1993
B-cell lymphoma of recipient origin 9 years after allogeneic bone marrow transplantation for T-cell acute lymphoblastic leukaemiaM S Trimble, J S Waye, I R Walker, et al.
Hemoglobin|April 13, 2001
Novel beta-thalassemia mutation in a beta-thalassemia intermedia patientJ S Waye, B Eng, M Patterson, et al.
The Journal of Laboratory and Clinical Medicine|October 1, 1991
High hemoglobin A2 beta-thalassemiaM H Steinberg, M B Coleman, J G Adams, et al.
The Journal of Pediatrics|May 29, 1998
Coinheritance of alpha-thalassemia-1 and hemoglobin E/beta zero-thalassemia: practical implications for neonatal screening and genetic counselingL Krishnamurti, D H Chui, M Dallaire, 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.
Hemoglobin|October 10, 1997
Novel mutation of the alpha 2-globin gene initiation codon (ATG-->A-G) in a Vietnamese girl with Hb H diseaseJ S Waye, B Eng, M Patterson, 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.
Pageof 12

Showing results (71-80 of 115) 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.
British Journal of Haematology|October 7, 2000
Compound heterozygosity for triplicated alpha-globin gene and (- -(SEA)) alpha-globin gene deletion: implication for thalassaemia screeningS K Ma, A Y Chan, L C CHan, et al.
American Journal of Hematology|February 3, 1999
A novel and de novo spontaneous point mutation (Glu271STOP) of the antithrombin gene results in a type I deficiency and thrombophiliaM D Tarantino, S M Curtis, G S Johnson, et al.
British Journal of Haematology|September 1, 1993
B-cell lymphoma of recipient origin 9 years after allogeneic bone marrow transplantation for T-cell acute lymphoblastic leukaemiaM S Trimble, J S Waye, I R Walker, et al.
Hemoglobin|April 13, 2001
Novel beta-thalassemia mutation in a beta-thalassemia intermedia patientJ S Waye, B Eng, M Patterson, et al.
The Journal of Laboratory and Clinical Medicine|October 1, 1991
High hemoglobin A2 beta-thalassemiaM H Steinberg, M B Coleman, J G Adams, et al.
The Journal of Pediatrics|May 29, 1998
Coinheritance of alpha-thalassemia-1 and hemoglobin E/beta zero-thalassemia: practical implications for neonatal screening and genetic counselingL Krishnamurti, D H Chui, M Dallaire, 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.
Hemoglobin|October 10, 1997
Novel mutation of the alpha 2-globin gene initiation codon (ATG-->A-G) in a Vietnamese girl with Hb H diseaseJ S Waye, B Eng, M Patterson, 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.
Pageof 12