A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization. [electronic resource]
Producer: 20160401Description: 703-8 p. digitalISSN:- 1873-2933
- Adult
- Base Sequence
- Chromosome Inversion -- genetics
- Epistasis, Genetic
- Female
- Gene Deletion
- Humans
- Male
- Middle Aged
- Molecular Sequence Data
- Multigene Family -- genetics
- Mutagenesis, Insertional
- Olfactory Receptor Neurons -- physiology
- Pedigree
- Phenotype
- Young Adult
- alpha-Thalassemia -- diagnosis
- beta-Globins -- genetics
- beta-Thalassemia -- diagnosis
- delta-Thalassemia -- diagnosis
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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