Literature DB >> 18615546

Molecular prenatal diagnosis of Hb H hydrops fetalis caused by haemoglobin Adana and the implications to antenatal screening for alpha-thalassaemia.

S Henderson, M Pitman, J McCarthy, A Molyneux, J Old.   

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Year:  2008        PMID： 18615546     DOI： 10.1002/pd.2045

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  3 in total

1.  Α case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α+- thalassemia deletion: guilty or innocent.

Authors:  A Tampaki; S Theodoridou; Ch Apostolou; E E Delaki; E Vlachaki
Journal:  Hippokratia       Date:  2020 Jan-Mar       Impact factor: 0.471

2.  Hydrops fetalis associated with homozygosity for Hb Adana [alpha59(E8)Gly-->Asp (alpha2)].

Authors:  Ita M Nainggolan; Alida Harahap; Iswari Setianingsih
Journal:  Hemoglobin       Date:  2010       Impact factor: 0.849

3.  Severe α-thalassemia intermedia due to a compound heterozygosity for the highly unstable Hb Adana (HBA2: c.179G>A) and a novel codon 24 (HBA2: c.75T>A) mutation.

Authors:  Dewi Megawati; Ita M Nainggolan; Maria Swastika; Susi Susanah; Johanes C Mose; Alida R Harahap; Iswari Setianingsih
Journal:  Hemoglobin       Date:  2013-12-18       Impact factor: 0.849
  3 in total

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