Literature DB >> 5915052

Thalassaemia types among Kurdish Jews in Israel.

A Horowitz, T Cohen, E Goldschmidt, C Levene.   

Abstract

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Year:  1966        PMID： 5915052     DOI： 10.1111/j.1365-2141.1966.tb00138.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  5 in total

1.  The Gm and Inv allotypes in kindreds of Kurdish Jews.

Authors:  A G Steinberg; C Levene; E Goldschmidt; T Cohen
Journal:  Am J Hum Genet       Date:  1970-11       Impact factor: 11.025

2.  Haemoglobin H disease in Arabs in Kuwait.

Authors:  S A Ali
Journal:  J Clin Pathol       Date:  1969-03       Impact factor: 3.411

3.  Diversity of beta-globin mutations in Israeli ethnic groups reflects recent historic events.

Authors:  D Filon; V Oron; S Krichevski; A Shaag; Y Shaag; T C Warren; A Goldfarb; Y Shneor; A Koren; M Aker
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

4.  G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews.

Authors:  A Oppenheim; C L Jury; D Rund; T J Vulliamy; L Luzzatto
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

5.  Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.

Authors:  D Rund; T Cohen; D Filon; C E Dowling; T C Warren; I Barak; E Rachmilewitz; H H Kazazian; A Oppenheim
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-01       Impact factor: 11.205
  5 in total

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