| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Angiotensin-converting enzyme (ACE) I/D and bradykinin B2 receptor T/C genes polymorphism in patients with ACE inhibitors-related cough
|
Rohman, Mohammad Saifur
|
|
2018
|
19 |
4 |
p. 307-313
|
artikel
|
| 2 |
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
|
Gravand, Abdollah
|
|
2018
|
19 |
4 |
p. 403-407
|
artikel
|
| 3 |
Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion
|
Çelik, Vesile Deniz
|
|
2018
|
19 |
4 |
p. 433-435
|
artikel
|
| 4 |
Cantu syndrome in an Egyptian child
|
Shawky, Rabah M.
|
|
2018
|
19 |
4 |
p. 429-432
|
artikel
|
| 5 |
Detection of antimicrobial resistance genes of Helicobacter pylori strains to clarithromycin, metronidazole, amoxicillin and tetracycline among Egyptian patients
|
Diab, Manal
|
|
2018
|
19 |
4 |
p. 417-423
|
artikel
|
| 6 |
Evaluation of health-related quality of life and muscular strength in children with beta thalassemia major
|
Ismail, Dina K.
|
|
2018
|
19 |
4 |
p. 353-357
|
artikel
|
| 7 |
FLT3 receptor/CD135 expression by flow cytometry in acute myeloid leukemia: Relation to FLT3 gene mutations and mRNA transcripts
|
Mekawy, Mohamed Amin
|
|
2018
|
19 |
4 |
p. 345-351
|
artikel
|
| 8 |
Fuzzy system model for gene expression
|
Sharma, Amit
|
|
2018
|
19 |
4 |
p. 301-306
|
artikel
|
| 9 |
Genetic study of the NOTCH3 gene in CADASIL patients
|
Chavoshi Tarzjani, Seyedeh Parisa
|
|
2018
|
19 |
4 |
p. 425-427
|
artikel
|
| 10 |
Helicobacter pylori Western cagA genotype in Egyptian patients with upper gastrointestinal disease
|
Diab, Manal
|
|
2018
|
19 |
4 |
p. 297-300
|
artikel
|
| 11 |
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
|
Al-Wakeel, Hanan
|
|
2018
|
19 |
4 |
p. 325-331
|
artikel
|
| 12 |
In silico analysis of the functional non-synonymous single nucleotide polymorphisms in the human CYP27B1 gene
|
Rotimi, Solomon O.
|
|
2018
|
19 |
4 |
p. 367-378
|
artikel
|
| 13 |
Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress
|
Youssef, Omneya Ibrahim
|
|
2018
|
19 |
4 |
p. 321-324
|
artikel
|
| 14 |
Metadherin mRNA expression in hepatocellular carcinoma
|
Al-sheikh, Nevein M.
|
|
2018
|
19 |
4 |
p. 391-397
|
artikel
|
| 15 |
MTHFR C677T polymorphism and risk of esophageal cancer: An updated meta-analysis
|
Kumar, Pradeep
|
|
2018
|
19 |
4 |
p. 273-284
|
artikel
|
| 16 |
New insights into smudge cell percentage in chronic lymphocytic Leukemia: A novel prognostic indicator of disease burden
|
Mohamed, Amal Abd El Hamid
|
|
2018
|
19 |
4 |
p. 409-415
|
artikel
|
| 17 |
Pathogenic predictions of non-synonymous variants and their impacts: A computational assessment of ARHGEF6 gene
|
Khimsuriya, Yashvant M.
|
|
2018
|
19 |
4 |
p. 333-344
|
artikel
|
| 18 |
Pathophysiology of bleeding diathesis in haemophilia-A: A sequential and critical appraisal of non-FVIII related haemostatic dysfunctions and their therapeutic implications
|
Ibrahim, Umma A.
|
|
2018
|
19 |
4 |
p. 285-295
|
artikel
|
| 19 |
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]
|
Elsayed, Solaf M.
|
|
2018
|
19 |
4 |
p. 443
|
artikel
|
| 20 |
Renalase gene polymorphisms (rs2576178 and rs10887800) in Egyptian hypertensive end stage renal disease patients
|
Kandil, Noha S.
|
|
2018
|
19 |
4 |
p. 379-383
|
artikel
|
| 21 |
Study of congenital malformations in infants and children in Menoufia governorate, Egypt
|
AbouEl-Ella, Soheir S.
|
|
2018
|
19 |
4 |
p. 359-365
|
artikel
|
| 22 |
Study of DNA methyl transferase 3A mutation in acute myeloid leukemic patients
|
Elsayed, Ghada M.
|
|
2018
|
19 |
4 |
p. 315-319
|
artikel
|
| 23 |
Study of the role of IL-17F gene polymorphism in the development of immune thrombocytopenia among the Egyptian children
|
Botros, Shahira K.A.
|
|
2018
|
19 |
4 |
p. 385-389
|
artikel
|
| 24 |
The cephalofacial characterization in humans: The study using igbo tribe in Nigeria
|
Obaje, Godwin Sunday
|
|
2018
|
19 |
4 |
p. 399-402
|
artikel
|
| 25 |
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
|
Silan, Fatma
|
|
2018
|
19 |
4 |
p. 437-441
|
artikel
|
Tijdschrift beschrijving