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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 5
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Original Article

HB H Disease and Mild Mental Retardation in a Black Girl with a HB S Heterozygosity

Y-J. Fei Departments of Biochemistry and Molecular Biology and Pediatric Hematology/Oncology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
J-C. Liu Departments of Biochemistry and Molecular Biology and Pediatric Hematology/Oncology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
V. C. McKie Departments of Biochemistry and Molecular Biology and Pediatric Hematology/Oncology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
T. H. J. Huisman Departments of Biochemistry and Molecular Biology and Pediatric Hematology/Oncology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
Pages 431-434 | Received 10 Apr 1992, Accepted 10 Jun 1992, Published online: 07 Jul 2009

Citations (4)

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Read on this site (1)

T. H. J. Huisman, L-H. Gu, J-C. Liu, Y-J. Fei & E. L.D. Walker. (1993) Black α-Thalassemia-1: Partial Characterization of an ∼80 KB Deletion Which Includes the ξ- and α-Globin Genes. Hemoglobin 17:4, pages 345-353.
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Articles from other publishers (3)

William T. Gibson, Chansonette Harvard, Ying Qiao, Martin J. Somerville, M.E. Suzanne Lewis & Evica Rajcan‐Separovic. (2007) Phenotype–genotype characterization of alpha‐thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3. American Journal of Medical Genetics Part A 146A:2, pages 225-232.
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Cornelis L. Harteveld, Marjolein Kriek, Emilia K. Bijlsma, Zoran Erjavec, Deepak Balak, Marion Phylipsen, Astrid Voskamp, Emmanora di Capua, Stefan J. White & Piero C. Giordano. (2007) Refinement of the genetic cause of ATR-16. Human Genetics 122:3-4, pages 283-292.
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Antonios C. Kattamis, Clara Camaschella, Piera Sivera, Saul Surrey & Paolo Fortina. (1998) Human α‐Thalassemia syndromes: Detection of molecular defects . American Journal of Hematology 53:2, pages 81-91.
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