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Hemoglobin
|
January 1, 1981
Hb Wuming or alpha 2 11(A9)Lys substituting for Gln beta 2
Y T Zeng, S Z Huang, L Xu, et al.
Hemoglobin
|
January 1, 1987
Hb Borås or alpha 2 beta 2(88)(F4)Leu----Arg in a South African female
A R Bird, T E Elliot, J B Wilson, et al.
Hemoglobin
|
January 1, 1981
Heterozygosity and homozygosity for the high oxygen affinity hemoglobin Tarrant or alpha 126 (H9) Asp replaced by Asn in two Mexican families
B Ibarra, G Vaca, J M Cantú, et al.
Hemoglobin
|
January 1, 1983
Hb A2-Manzanares or alpha 2 delta 2 121 (GH4) Glu replaced by Val, an unstable delta chain variant observed in a Spanish family
C Romero Garcia, J L Navarro, H Lam, et al.
The Journal of Clinical Investigation
|
March 1, 1971
Hemoglobin Savannah (B6(24) beta-glycine is greater than valine): an unstable variant causing anemia with inclusion bodies
T H Huisman, A K Brown, G D Efremov, et al.
Hemoglobin
|
January 1, 1978
Hemoglobin Hofu or alpha 2 beta 2 [126 (H4) Va1 leads to Glu] found in combination with hemoglobin S
G Brittenham, B Lozoff, J W Harris, et al.
Biochimica Et Biophysica Acta
|
April 29, 1975
Hemoglobin Atlanta or alpha 2 beta 2 75 Leu-Pro (E19): an unstable variant found in several members of a Caucasian family
M Hubbard, E F Winton, J G Lindeman, et al.
Hemoglobin
|
December 1, 1993
Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatography
D D Pobedimskaya, T P Molchanova, R Amernick, et al.
Hemoglobin
|
January 1, 1989
Two rare unstable beta chain variants, Hb Mozhaisk or alpha 2 beta 292(F8)His----Arg and Hb Djelfa or alpha 2 beta 298(Fg5)Val----Ala, each being observed for the second time
A R Bird, T Elliott, J B Wilson, et al.
Biochimica Et Biophysica Acta
|
December 10, 1992
Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia
V Divoky, E Bissé, J B Wilson, et al.
Page
of 37
Search research articles
Search
Showing results (261-270 of 363) with videos related to
Sort By:
Page
of 37
Hemoglobin
|
January 1, 1981
Hb Wuming or alpha 2 11(A9)Lys substituting for Gln beta 2
Y T Zeng, S Z Huang, L Xu, et al.
Hemoglobin
|
January 1, 1987
Hb Borås or alpha 2 beta 2(88)(F4)Leu----Arg in a South African female
A R Bird, T E Elliot, J B Wilson, et al.
Hemoglobin
|
January 1, 1981
Heterozygosity and homozygosity for the high oxygen affinity hemoglobin Tarrant or alpha 126 (H9) Asp replaced by Asn in two Mexican families
B Ibarra, G Vaca, J M Cantú, et al.
Hemoglobin
|
January 1, 1983
Hb A2-Manzanares or alpha 2 delta 2 121 (GH4) Glu replaced by Val, an unstable delta chain variant observed in a Spanish family
C Romero Garcia, J L Navarro, H Lam, et al.
The Journal of Clinical Investigation
|
March 1, 1971
Hemoglobin Savannah (B6(24) beta-glycine is greater than valine): an unstable variant causing anemia with inclusion bodies
T H Huisman, A K Brown, G D Efremov, et al.
Hemoglobin
|
January 1, 1978
Hemoglobin Hofu or alpha 2 beta 2 [126 (H4) Va1 leads to Glu] found in combination with hemoglobin S
G Brittenham, B Lozoff, J W Harris, et al.
Biochimica Et Biophysica Acta
|
April 29, 1975
Hemoglobin Atlanta or alpha 2 beta 2 75 Leu-Pro (E19): an unstable variant found in several members of a Caucasian family
M Hubbard, E F Winton, J G Lindeman, et al.
Hemoglobin
|
December 1, 1993
Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatography
D D Pobedimskaya, T P Molchanova, R Amernick, et al.
Hemoglobin
|
January 1, 1989
Two rare unstable beta chain variants, Hb Mozhaisk or alpha 2 beta 292(F8)His----Arg and Hb Djelfa or alpha 2 beta 298(Fg5)Val----Ala, each being observed for the second time
A R Bird, T Elliott, J B Wilson, et al.
Biochimica Et Biophysica Acta
|
December 10, 1992
Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia
V Divoky, E Bissé, J B Wilson, et al.
Page
of 37