Literature DB >> 1694572

Hemoglobin Bart's disease in an Italian boy. Interaction between alpha-thalassemia and hereditary persistence of fetal hemoglobin.

D H Chui1, M Patterson, C E Dowling, H H Kazazian, A G Kendall.   

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Year:  1990        PMID： 1694572     DOI： 10.1056/NEJM199007193230307

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  3 in total

1.  Assembly of recently translated full-length and C-terminal truncated human gamma-globin chains with a pool of alpha-globin chains to form Hb F in a cell-free system.

Authors:  Kazuhiko Adachi; Yi Zhao; Vinaysagar Lakka; Mitchell J Weiss; Saul Surrey
Journal:  Arch Biochem Biophys       Date:  2007-03-16       Impact factor: 4.013

2.  The thalassemias and health care in Canada: a place for genetics in medicine.

Authors:  D H Chui; S C Wong; C R Scriver
Journal:  CMAJ       Date:  1991-01-01       Impact factor: 8.262

Review 3.  Classification of the disorders of hemoglobin.

Authors:  Bernard G Forget; H Franklin Bunn
Journal:  Cold Spring Harb Perspect Med       Date:  2013-02-01       Impact factor: 6.915
  3 in total

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