Literature DB >> 35045200

Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)0 -thalassemia deletion.

Banu Aygun1, Adriana Bello2, Alexis A Thompson3, Lance Davis4, Yanan Sun4, Hong-Yuan Luo4, Shuaiying Cui4, David H K Chui4.   

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Year:  2022        PMID: 35045200     DOI: 10.1002/ajh.26470

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


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  1 in total

1.  Microcytic Anemia: An Insidious Presentation of Sickle Cell Beta+ Thalassemia, a Rare Sickle Cell Variant.

Authors:  Malavika Shankar; Nicole Gousy; Tutul Chowdhury
Journal:  Cureus       Date:  2022-03-18
  1 in total

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