Literature DB >> 18492098

The deletion of SOX8 is not associated with ATR-16 in an HbH family from Brazil.

M A C B Bezerra, A S Araujo, M Phylipsen, D Balak, E M Kimura, D M Oliveira, F F Costa, M F Sonati, C L Harteveld.   

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Year:  2008        PMID： 18492098     DOI： 10.1111/j.1365-2141.2008.07187.x

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


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  4 in total

1.  Two atypical forms of HbH disease in Sardinia.

Authors:  Maria Elisabetta Paglietti; Maria Carla Sollaino; Daniela Loi; Francesca Sarra; Eleonora Zaccheddu; Renzo Galanello
Journal:  Haematologica       Date:  2011-07-12       Impact factor: 9.941

2.  The molecular basis of α-thalassemia.

Authors:  Douglas R Higgs
Journal:  Cold Spring Harb Perspect Med       Date:  2013-01-01       Impact factor: 6.915

3.  α-Thalassemia, mental retardation, and myelodysplastic syndrome.

Authors:  Richard J Gibbons
Journal:  Cold Spring Harb Perspect Med       Date:  2012-10-01       Impact factor: 6.915

4.  ATR-16 syndrome: mechanisms linking monosomy to phenotype.

Authors:  Christian Babbs; Jill Brown; Sharon W Horsley; Joanne Slater; Evie Maifoshie; Shiwangini Kumar; Paul Ooijevaar; Marjolein Kriek; Amanda Dixon-McIver; Cornelis L Harteveld; Jan Traeger-Synodinos; Andrew O M Wilkie; Douglas R Higgs; Veronica J Buckle
Journal:  J Med Genet       Date:  2020-01-31       Impact factor: 6.318
  4 in total

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