Literature DB >> 4743438

The clinical and haematological findings in children inheriting two types of thalassaemia: high-A2, type beta-thalassaemia, and high-F type or delta beta-thalassaemia.

C Kattamis, A Metaxotou-Mavromati, K Karamboula, E Nasika, H Lehmann.   

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Year:  1973        PMID： 4743438     DOI： 10.1111/j.1365-2141.1973.tb01748.x

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


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  4 in total

1.  Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis.

Authors:  J M Cantú; B Ibarra; G Vaca; M L Ramirez; J Sánchez-Corona
Journal:  Hum Genet       Date:  1979-06-19       Impact factor: 4.132

2.  Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.

Authors:  L Cianetti; A Care; N M Sposi; A Giampaolo; M Calandrini; M Petrini; A Massa; M Marinucci; F Mavilio; M Ceccanti
Journal:  J Med Genet       Date:  1984-08       Impact factor: 6.318

3.  The clinical phenotype of beta and delta beta thalassemias in Greece.

Authors:  C Kattamis; A Metaxotou-Mavromati; V Ladis; H Tsiarta; S Laskari; E Kanavakis
Journal:  Eur J Pediatr       Date:  1982-10       Impact factor: 3.183

4.  Delta beta (F)-thalassaemia in Sardinia.

Authors:  A Cao; M A Melis; R Galanello; A Angius; M Furbetta; P Giordano; L F Bernini
Journal:  J Med Genet       Date:  1982-06       Impact factor: 6.318
  4 in total

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