Literature DB >> 474574

The association of sickle cell anemia with heterozygous and homozygous alpha-thalassemia-2: in vitro HB chain synthesis.

A E Felice, B Webber, A Miller, S M Mayson, H F Harris, J B Henson, M E Gravely, T H Huisman.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1979        PMID： 474574     DOI： 10.1002/ajh.2830060202

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


× No keyword cloud information.
  5 in total

1.  Heterogeneity of sickle-cell anemia based on a profile of hematological variables.

Authors:  D J Odenheimer; C F Whitten; D L Rucknagel; S A Sarnaik; C F Sing
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025

2.  Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.

Authors:  A E Felice; R Ozdonmez; M E Headlee; T H Huisman
Journal:  Biochem Genet       Date:  1982-08       Impact factor: 1.890

3.  Alpha-thalassemia and the production of different alpha chain variants in heterozygotes.

Authors:  A E Felice; B B Webber; T H Huisman
Journal:  Biochem Genet       Date:  1981-06       Impact factor: 1.890

4.  Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.

Authors:  Irene Lubega; Christopher M Ndugwa; Edison A Mworozi; James K Tumwine
Journal:  Afr Health Sci       Date:  2015-06       Impact factor: 0.927

5.  Iron deficiency in sickle cell anaemia.

Authors:  S Davies; J Henthorn; M Brozović
Journal:  J Clin Pathol       Date:  1983-09       Impact factor: 3.411
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.