Found: 25
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MTHFR C677T polymorphism and risk of esophageal cancer: An updated meta-analysis.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 273, doi. 10.1016/j.ejmhg.2018.04.003
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- Publication type:
- Article
Pathophysiology of bleeding diathesis in haemophilia-A: A sequential and critical appraisal of non-FVIII related haemostatic dysfunctions and their therapeutic implications.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 285, doi. 10.1016/j.ejmhg.2018.01.003
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- Publication type:
- Article
Helicobacter pylori Western cagA genotype in Egyptian patients with upper gastrointestinal disease.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 297, doi. 10.1016/j.ejmhg.2018.06.003
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- Publication type:
- Article
Fuzzy system model for gene expression.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 301, doi. 10.1016/j.ejmhg.2018.06.002
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- Publication type:
- Article
Angiotensin-converting enzyme (ACE) I/D and bradykinin B2 receptor T/C genes polymorphism in patients with ACE inhibitors-related cough.
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- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 307, doi. 10.1016/j.ejmhg.2018.05.006
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- Publication type:
- Article
Study of DNA methyl transferase 3A mutation in acute myeloid leukemic patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 315, doi. 10.1016/j.ejmhg.2018.05.005
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- Publication type:
- Article
Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 321, doi. 10.1016/j.ejmhg.2018.05.004
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- Publication type:
- Article
Impact of PAI-1 4G/5G and C > G polymorphisms in acute ST elevation myocardial infarction and stable angina patients: A single center Egyptian study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 325, doi. 10.1016/j.ejmhg.2018.05.003
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- Publication type:
- Article
Pathogenic predictions of non-synonymous variants and their impacts: A computational assessment of ARHGEF6 gene.
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- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 333, doi. 10.1016/j.ejmhg.2018.05.002
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- Publication type:
- Article
FLT3 receptor/CD135 expression by flow cytometry in acute myeloid leukemia: Relation to FLT3 gene mutations and mRNA transcripts.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 345, doi. 10.1016/j.ejmhg.2018.04.006
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- Publication type:
- Article
Evaluation of health-related quality of life and muscular strength in children with beta thalassemia major.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 353, doi. 10.1016/j.ejmhg.2018.04.005
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- Publication type:
- Article
Study of congenital malformations in infants and children in Menoufia governorate, Egypt.
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- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 359, doi. 10.1016/j.ejmhg.2018.04.002
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- Publication type:
- Article
In silico analysis of the functional non-synonymous single nucleotide polymorphisms in the human CYP27B1 gene.
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- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 367, doi. 10.1016/j.ejmhg.2018.03.001
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- Publication type:
- Article
Renalase gene polymorphisms (rs2576178 and rs10887800) in Egyptian hypertensive end stage renal disease patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 379, doi. 10.1016/j.ejmhg.2018.02.004
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- Publication type:
- Article
Study of the role of IL-17F gene polymorphism in the development of immune thrombocytopenia among the Egyptian children.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 385, doi. 10.1016/j.ejmhg.2018.02.003
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- Publication type:
- Article
Metadherin mRNA expression in hepatocellular carcinoma.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 391, doi. 10.1016/j.ejmhg.2018.02.002
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- Publication type:
- Article
The cephalofacial characterization in humans: The study using igbo tribe in Nigeria.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 399, doi. 10.1016/j.ejmhg.2018.02.001
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- Publication type:
- Article
A study on the association of TCF7L2 rs11196205 (C/G) and CAPN10 rs3792267 (G/A) polymorphisms with type 2 diabetes mellitus in the South Western of Iran.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 403, doi. 10.1016/j.ejmhg.2018.01.007
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- Publication type:
- Article
New insights into smudge cell percentage in chronic lymphocytic Leukemia: A novel prognostic indicator of disease burden.
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- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 409, doi. 10.1016/j.ejmhg.2018.01.006
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- Publication type:
- Article
Detection of antimicrobial resistance genes of Helicobacter pylori strains to clarithromycin, metronidazole, amoxicillin and tetracycline among Egyptian patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 417, doi. 10.1016/j.ejmhg.2018.01.004
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- Publication type:
- Article
Genetic study of the NOTCH3 gene in CADASIL patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 425, doi. 10.1016/j.ejmhg.2018.05.001
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- Publication type:
- Article
Cantu syndrome in an Egyptian child.
- Published in:
- 2018
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- Publication type:
- Case Study
Asymptomatic hemochromatosis case with HFE c.1007-47G>A, c.340+4T>C heterozygous mutations and alpha globin -3.7 kb deletion.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report.
- Published in:
- 2018
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- Publication type:
- Case Study
Removal notice to "An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings" [Egypt J Med Hum Genet 18 (2017) 393-396].
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 443, doi. 10.1016/j.ejmhg.2018.04.004
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- Publication type:
- Article