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Hemoglobin
international journal for hemoglobin research
Volume 20, 1996 - Issue 1
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Miscellaneous Article

Hb J-Baltimore [β16(A13)GLY→ASP] Associated with β+Thalassemia in a Spanish Family

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Pages 79-84 | Received 01 May 1995, Accepted 15 Nov 1995, Published online: 07 Jul 2009

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Jialing Cui, Christoph Baysdorfer, Mahin Azimi, Elliott P. Vichinsky & Carolyn C. Hoppe. (2012) Identification of Three Novel Hb F Variants: Hb F-Hayward [Gγ1(NA1)Gly→Asp, GGT>GAT], Hb F-Chori-I [AγT16(A13)Gly→Asp, GGC>GAC] and Hb F-Chori-II [AγI29(B11)Gly→Glu, GGA>GAA]. Hemoglobin 36:3, pages 305-309.
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NE Larocca González, MA Álvarez Rueda, EM Deschamps Mosquera & FJ Peteiro-Cartelle. (2023) Detección de la Hb J-Baltimore durante la medición de la HbA1c por HPLC. Revista de Medicina de Laboratorio.
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Manuel A. Gargallo, Fernando Ataulfo González & Ana Villegas. (2010) Abnormally low HbA1c secondary to hemoglobin J-Baltimore [beta 16(A13) Gly→Asp]. Family study. Endocrinología y Nutrición 57:2, pages 83-85.
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Ossama Barakat, S.T. Murali Krishnan & Ketan Dhatariya. (2008) Falsely low HbA1c value due to a rare variant of hemoglobin J-Baltimore. Primary Care Diabetes 2:3, pages 155-157.
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Upendra Srinivas, Manoranjan Mahapatra & H.P. Pati. (2006) Hb J Meerut, a fast‐moving hemoglobin—a study of seven cases from India and a review of literature. American Journal of Hematology 82:7, pages 666-667.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .

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