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J S Waye

Showing results (101-110 of 115) with videos related to

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The New England Journal of Medicine|May 1, 1997
Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screeningY L Lau, L C Chan, Y Y Chan, et al.
American Journal of Hematology|September 1, 1995
Severity of beta-thalassemia due to genotypes involving the IVS-I-6 (T-->C) mutationJ S Waye, B Eng, M Patterson, et al.
American Journal of Hematology|December 1, 1994
Hb E/Hb LeporeHollandia in a family from BangladeshJ S Waye, B Eng, M Patterson, et al.
Lancet (London, England)|August 16, 1997
Treatment of thalassaemia major with phenylbutyrate and hydroxyureaN F Olivieri, D C Rees, G D Ginder, et al.
British Journal of Haematology|November 28, 2001
Hb H hydrops foetalis syndrome: a case report and review of literatureF Lorey, P Charoenkwan, H E Witkowska, et al.
Hemoglobin|September 18, 1999
Spectrum of beta-thalassemia mutations in EgyptJ S Waye, S Borys, B Eng, et al.
Blood|July 15, 1992
Human embryonic zeta-globin chain expression in deletional alpha-thalassemiasW Tang, H Y Luo, M Albitar, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Elimination of transfusions through induction of fetal hemoglobin synthesis in Cooley's anemiaN F Olivieri, D C Rees, G D Ginder, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 10, 2017
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutationM S Badin, J K Iyer, M Chong, et al.
Clinical Genetics|November 4, 2004
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndromeE Ciara, M J M Nowaczyk, M Witsch-Baumgartner, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
The New England Journal of Medicine|May 1, 1997
Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screeningY L Lau, L C Chan, Y Y Chan, et al.
American Journal of Hematology|September 1, 1995
Severity of beta-thalassemia due to genotypes involving the IVS-I-6 (T-->C) mutationJ S Waye, B Eng, M Patterson, et al.
American Journal of Hematology|December 1, 1994
Hb E/Hb LeporeHollandia in a family from BangladeshJ S Waye, B Eng, M Patterson, et al.
Lancet (London, England)|August 16, 1997
Treatment of thalassaemia major with phenylbutyrate and hydroxyureaN F Olivieri, D C Rees, G D Ginder, et al.
British Journal of Haematology|November 28, 2001
Hb H hydrops foetalis syndrome: a case report and review of literatureF Lorey, P Charoenkwan, H E Witkowska, et al.
Hemoglobin|September 18, 1999
Spectrum of beta-thalassemia mutations in EgyptJ S Waye, S Borys, B Eng, et al.
Blood|July 15, 1992
Human embryonic zeta-globin chain expression in deletional alpha-thalassemiasW Tang, H Y Luo, M Albitar, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Elimination of transfusions through induction of fetal hemoglobin synthesis in Cooley's anemiaN F Olivieri, D C Rees, G D Ginder, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 10, 2017
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutationM S Badin, J K Iyer, M Chong, et al.
Clinical Genetics|November 4, 2004
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndromeE Ciara, M J M Nowaczyk, M Witsch-Baumgartner, et al.
Pageof 12