Connection

Miguel Abboud to Mutation

This is a "connection" page, showing publications Miguel Abboud has written about Mutation.
Connection Strength

0.627
  1. Alpha thalassemia allelic frequency in Lebanon. Pediatr Blood Cancer. 2015 Jan; 62(1):120-2.
    View in: PubMed
    Score: 0.320
  2. The Spectrum of ?-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study. Hemoglobin. 2021 Nov; 45(6):365-370.
    View in: PubMed
    Score: 0.126
  3. Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutation. Pediatr Blood Cancer. 2008 Jan; 50(1):113-4.
    View in: PubMed
    Score: 0.050
  4. Diagnosis and Treatment of a Patient With Severe Combined Immunodeficiency Due to a Novel Homozygous Mutation in the IL-7Ra Chain. Front Immunol. 2022; 13:867837.
    View in: PubMed
    Score: 0.034
  5. Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived From Structural and Functional Analysis of 14 ClC-7 Mutants. J Bone Miner Res. 2021 03; 36(3):531-545.
    View in: PubMed
    Score: 0.031
  6. Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon. Clin Immunol. 2020 10; 219:108573.
    View in: PubMed
    Score: 0.030
  7. Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis. Genome Med. 2015 Dec 18; 7:130.
    View in: PubMed
    Score: 0.022
  8. Vascular at-risk genotypes and disease severity in Lebanese sickle cell disease patients. Am J Hematol. 2010 May; 85(5):395-6.
    View in: PubMed
    Score: 0.015
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.