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Hemoglobin|June 1, 1993
Expediting rare variant hemoglobin characterization by combined HPLC/electrospray mass spectrometryH E Witkowska, F Bitsch, C H ShackletonHemoglobin|November 1, 1994
A rodent model for hemoglobin switching utilizing high performance liquid chromatographyJ T Pearson, J Enriquez, W Critz, et al.Hemoglobin|September 26, 2001
A novel splice acceptor site mutation of the alpha2-globin gene causing alpha-thalassemiaN I Noguera, F A González, R A Dávoli, et al.Hemoglobin|January 1, 1986
Functional activity of the triplicated alpha alpha alpha 4.2/gene rearrangementR J Trent, J Yakas, P E Brock, et al.Hemoglobin|January 1, 1986
The identification of five rare beta-chain abnormal hemoglobins by high performance liquid chromatographic proceduresJ B Wilson, S S Chen, B B Webber, et al.Hemoglobin|January 1, 1987
A new case of Hb Little Rock [beta 143(H21)His----Gln], a high affinity variant. Study during pregnancyA Francina, C Lacombe, F Baklouti, et al.Hemoglobin|December 20, 2014
Identification of nondeletional α-thalassemia in a prenatal screening program by reverse dot-blot in southern ChinaJian Li, Ru Li, Dong-Zhi LiHemoglobin|October 16, 2014
Prenatal control of Hb Bart's disease in mainland China: can we do better?Ping He, Yu Yang, Ru Li, et al.Hemoglobin|November 4, 2015
Characterization of the HBB: c.*233G > C Variant: No Evidence of a β-Thalassemic PhenotypeDebra L Smith, Midori Mitui, Jason Y Park, et al.Hemoglobin|November 5, 2015
Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 GeneSamaneh Farashi, Shadi Vakili, Negin F Garous, et al.Pageof 238