Literature DB >> 6155503

The varied arrangement of the alpha globin genes in alpha thalassemia and Hb H disease in American blacks.

G B Sancar, M M Cedeno, R F Rieder.   

Abstract

Both Eco RI and Eco RI x Bam HI restriction endonuclease digests of DNA from black Americans with alpha thalassemia yielded an alpha-specific fragment 4 kb shorter than in normals. In Hb H disease, only the shorter fragment was noted, while in "silent carriers" (alpha-thal 2 trait), both the normal and shorter fragments were detected. One subject with single gene deletions on both homologous chromosomes (alpha-thal 1 phe. A non-deletional form of alpha thalassemia also was discovered.

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Year:  1980        PMID: 6155503

Source DB:  PubMed          Journal:  Johns Hopkins Med J        ISSN: 0021-7263


  3 in total

1.  Extremely high frequencies of alpha-globin gene deletion in Madang and on Kar Kar Island, Papua New Guinea.

Authors:  P T Yenchitsomanus; K M Summers; K K Bhatia; J Cattani; P G Board
Journal:  Am J Hum Genet       Date:  1985-07       Impact factor: 11.025

Review 2.  The thalassemias: molecular mechanisms of human genetic disease.

Authors:  R A Spritz; B G Forget
Journal:  Am J Hum Genet       Date:  1983-05       Impact factor: 11.025

3.  Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletions.

Authors:  G B Sancar; B Tatsis; M M Cedeno; R F Rieder
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

  3 in total

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