HB monroe or α2β230(b12)ARG→THR, a variant associated with βthalassemia due to a g→c substitution adjacent to the donor splice site of the first intron

J. M. Gonzalez-Redondo, T. A. Stoming, F. Kutlar, Abdullah Kutlar, H. Hu, J. B. Wilson, T. H J Huisman

Research output: Contribution to journalArticle

31 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)67-74
Number of pages8
JournalHemoglobin
Volume13
Issue number1
DOIs
StatePublished - Jan 1 1989

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DNA Mutational Analysis
Abnormal Hemoglobins
RNA Splice Sites
Thalassemia
Gene Rearrangement
DNA Restriction Enzymes
DNA Probes
Multigene Family
Introns
Mutation

ASJC Scopus subject areas

  • Hematology
  • Genetics(clinical)
  • Clinical Biochemistry
  • Biochemistry, medical
  • Biochemistry

Cite this

HB monroe or α2β230(b12)ARG→THR, a variant associated with βthalassemia due to a g→c substitution adjacent to the donor splice site of the first intron. / Gonzalez-Redondo, J. M.; Stoming, T. A.; Kutlar, F.; Kutlar, Abdullah; Hu, H.; Wilson, J. B.; Huisman, T. H J.

In: Hemoglobin, Vol. 13, No. 1, 01.01.1989, p. 67-74.

Research output: Contribution to journalArticle

Gonzalez-Redondo, J. M. ; Stoming, T. A. ; Kutlar, F. ; Kutlar, Abdullah ; Hu, H. ; Wilson, J. B. ; Huisman, T. H J. / HB monroe or α2β230(b12)ARG→THR, a variant associated with βthalassemia due to a g→c substitution adjacent to the donor splice site of the first intron. In: Hemoglobin. 1989 ; Vol. 13, No. 1. pp. 67-74.
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