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Hemoglobin
international journal for hemoglobin research
Volume 19, 1995 - Issue 5
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Original Article

Hb S-Hb Lufkin Dise in A Black Male Infant

L-H. Gu Laboratory of Protein Chemistry Department of Biochemistry, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
J. Ye. Leonova Laboratory of Protein Chemistry Department of Biochemistry, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
T. H.J. Huisman Laboratory of Protein Chemistry Department of Biochemistry, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
Pages 291-294 | Received 08 Feb 1995, Accepted 31 May 1995, Published online: 07 Jul 2009

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Read on this site (3)

Chi-Chiu So, Amy Y.Y. Chan, Hong-Yuan Luo, Madeleine Verhovsek, David H.K. Chui, Siu-Cheung Ling & Li-Chong Chan. (2011) Hb A2 Hong Kong – A Novel δ-Globin Variant in a Chinese Family Masks the Diagnosis of β-Thalassemia Trait. Hemoglobin 35:2, pages 162-165.
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Philippe Lacan, Michel Becchi, Isabelle Zanella‐Cleon, Martine Aubry, Martine Ffrench, Nicole Couprie & Alain Francina. (2004) Two New β Chain Variants: Hb Tripoli [β26(B8)Glu→Ala] and Hb Tizi‐Ouzou [β29(B11)Gly→Ser]. Hemoglobin 28:3, pages 205-212.
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Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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Articles from other publishers (2)

Peihong Hsu, Ding Wen Wu, Ahna M. Blutreich, Paul J. Kurtin, James D. Hoyer & Gungor Karayalcin. (2009) Spontaneous Mutation of Hemoglobin Lufkin in a White Boy. Journal of Pediatric Hematology/Oncology 31:4, pages 281-284.
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Titus Hendrik Jan Huisman. (1997) Combinations of β chain abnormal hemoglobins with each other or with β-thalassemia determinants with known mutations: influence on phenotype. Clinical Chemistry 43:10, pages 1850-1856.
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