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L H Gu

Showing results (21-30 of 79) with videos related to

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Blood|June 15, 1996
A newly discovered frameshift at codons 120-121 (+A) of the beta gene is not associated with a dominant form of beta-thalassemiaP Hopmeier, W Krugluger, L H Gu, et al.
American Journal of Hematology|September 1, 1995
Hb Lulu Island (alpha 2 beta 2 107[G9]Gly-->Asp)-beta zero- thalassemia (codon 15; TGG-->TAG), a form of thalassemia intermediaG R Gray, H E Manson, L H Gu, et al.
British Journal of Haematology|March 1, 1993
A new beta zero-thalassaemia nonsense mutation (codon 112, T-->A) not associated with a dominant type of thalassaemia in the heterozygoteV Divoky, L H Gu, K Indrak, et al.
Acta Haematologica|January 1, 1997
Hydroxyurea therapy in sickle cell anemia patients in Curaçao, The Netherlands AntillesA W Saleh, H J Velvis, L H Gu, et al.
Hemoglobin|May 1, 1996
Hb Sögn or alpha 2 beta 2 14(A11)Leu-->Arg in combination with an alpha-thalassemia heterozygosityD R Miller, N S Smetanina, L H Gu, et al.
Hemoglobin|August 1, 1993
Black alpha-thalassemia-1: partial characterization of an approximately 80 kb deletion which includes the zeta- and alpha-globin genesT H Huisman, L H Gu, J C Liu, et al.
American Journal of Hematology|December 1, 1992
Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemiaG Schiliro, P Samperi, R Testa, et al.
Blood|September 15, 1990
Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variantJ F Codrington, H W Li, F Kutlar, et al.
British Journal of Haematology|June 1, 1996
The dominant beta-thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon ( = arginine) at the 5' end of the second exonS N Arjona, J M Eloy-Garcia, L H Gu, et al.
Hemoglobin|January 1, 1990
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adultD Plaseska, L H Gu, J B Wilson, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
Blood|June 15, 1996
A newly discovered frameshift at codons 120-121 (+A) of the beta gene is not associated with a dominant form of beta-thalassemiaP Hopmeier, W Krugluger, L H Gu, et al.
American Journal of Hematology|September 1, 1995
Hb Lulu Island (alpha 2 beta 2 107[G9]Gly-->Asp)-beta zero- thalassemia (codon 15; TGG-->TAG), a form of thalassemia intermediaG R Gray, H E Manson, L H Gu, et al.
British Journal of Haematology|March 1, 1993
A new beta zero-thalassaemia nonsense mutation (codon 112, T-->A) not associated with a dominant type of thalassaemia in the heterozygoteV Divoky, L H Gu, K Indrak, et al.
Acta Haematologica|January 1, 1997
Hydroxyurea therapy in sickle cell anemia patients in Curaçao, The Netherlands AntillesA W Saleh, H J Velvis, L H Gu, et al.
Hemoglobin|May 1, 1996
Hb Sögn or alpha 2 beta 2 14(A11)Leu-->Arg in combination with an alpha-thalassemia heterozygosityD R Miller, N S Smetanina, L H Gu, et al.
Hemoglobin|August 1, 1993
Black alpha-thalassemia-1: partial characterization of an approximately 80 kb deletion which includes the zeta- and alpha-globin genesT H Huisman, L H Gu, J C Liu, et al.
American Journal of Hematology|December 1, 1992
Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemiaG Schiliro, P Samperi, R Testa, et al.
Blood|September 15, 1990
Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variantJ F Codrington, H W Li, F Kutlar, et al.
British Journal of Haematology|June 1, 1996
The dominant beta-thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon ( = arginine) at the 5' end of the second exonS N Arjona, J M Eloy-Garcia, L H Gu, et al.
Hemoglobin|January 1, 1990
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adultD Plaseska, L H Gu, J B Wilson, et al.
Pageof 8