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HHEX gene polymorphisms and type 2 diabetes mellitus: A case‐control report from Iran.
- Published in:
- Journal of Cellular Biochemistry, 2019, v. 120, n. 10, p. 16445, doi. 10.1002/jcb.28788
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- Article
How to Assess Founder Effect in Patients with Congenital Factor XIII Deficiency.
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- International Journal of Hematology-Oncology & Stem Cell Research, 2020, v. 14, n. 4, p. 248
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- Article
Indirect Molecular Diagnosis of Congenital Factor XIII Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms.
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- Iranian Journal of Pediatric Hematology & Oncology, 2020, v. 10, n. 2, p. 114
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- Article
Whole Exome Sequencing for Mutation Screening in Hemophagocytic Lymphohistiocytosis.
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- Iranian Journal of Pediatric Hematology & Oncology, 2020, v. 10, n. 1, p. 38
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- Article
Whole Exome Sequencing of an X-linked Thrombocytopenia Patient with Normal Sized Platelets.
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- Avicenna Journal of Medical Biotechnology, 2019, v. 11, n. 3, p. 253
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- Article
CRISPR/Cas9, a promising approach for the treatment of β-thalassemia: a systematic review.
- Published in:
- Molecular Genetics & Genomics, 2023, v. 298, n. 1, p. 1, doi. 10.1007/s00438-022-01978-z
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- Article