Vol. 19 No. 4 (2018) | Egyptian Journal of Medical Human Genetics

MTHFR C677T polymorphism and risk of esophageal cancer: An updated meta-analysis

Pradeep Kumar, Vandana Rai

273-284

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Pathophysiology of bleeding diathesis in haemophilia-A: A sequential and critical appraisal of non-FVIII related haemostatic dysfunctions and their therapeutic implications

Umma A. Ibrahim, Sagir G. Ahmed

285-295

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Helicobacter pylori Western cagA genotype in Egyptian patients with upper gastrointestinal disease

Manal Diab, Mohamed Shemis, Doaa Gamal, Ahmed El-Shenawy, Maged El-Ghannam, Effat El-Sherbini, Mohamed Saber

297-300

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Fuzzy system model for gene expression

Amit Sharma, Neeru Adlakha

301-306

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Angiotensin-converting enzyme (ACE) I/D and bradykinin B2 receptor T/C genes polymorphism in patients with ACE inhibitors-related cough

Mohammad Saifur Rohman, Jonny Karunia Fajar, Bagus Hery Kuncahyo, Lowry Yunita, Erdo Puncak Sidarta, Putu Nina Belinda Saka, Teuku Heriansyah, Nashi Widodo

307-313

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Study of DNA methyl transferase 3A mutation in acute myeloid leukemic patients

Ghada M. Elsayed, Abd Elgawad A. Fahmi, Nevine F. Shafik, Reham A.A. Elshimy, Heba K. Abd Elhakeem, Sara A. Attea

315-319

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Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress

Omneya Ibrahim Youssef, Soha Youssef Raouf

321-324

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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

Hanan Al-Wakeel, Nadia Sewelam, Mohamed Khaled, Akram Abdelbary

325-331

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Pathogenic predictions of non-synonymous variants and their impacts: A computational assessment of ARHGEF6 gene

Yashvant M. Khimsuriya, Jenabhai B. Chauhan

333-344

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FLT3 receptor/CD135 expression by flow cytometry in acute myeloid leukemia: Relation to FLT3 gene mutations and mRNA transcripts

Mohamed Amin Mekawy, Deena Samir Eissa, Mohamed Tarif Hamza, Gehan Mostafa Hamed, Mariam Karam Youssef

345-351

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Evaluation of health-related quality of life and muscular strength in children with beta thalassemia major

Dina K. Ismail, Mona H. El-Tagui, Zeinab A. Hussein, Mohamed A. Eid, Sobhy M. Aly

353-357

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Study of congenital malformations in infants and children in Menoufia governorate, Egypt

Soheir S. AbouEl-Ella, Maha A. Tawfik, Wafaa Moustafa M. Abo El-Fotoh, Mai A. Elbadawi

359-365

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In silico analysis of the functional non-synonymous single nucleotide polymorphisms in the human CYP27B1 gene

Solomon O. Rotimi, Olamide Peter, Oluwayomi Oguntade, Oluwakemi A. Rotimi

367-378

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Renalase gene polymorphisms (rs2576178 and rs10887800) in Egyptian hypertensive end stage renal disease patients

Noha S. Kandil, Rania Mohamed El Sharkawy, Lubna Mohamed Ibrahim Desouky, Lamia Said Kandil, I.M. Masoud, Noha Gaber Amin

379-383

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Study of the role of IL-17F gene polymorphism in the development of immune thrombocytopenia among the Egyptian children

Shahira K.A. Botros, Ola M. Ibrahim, Alaa A. Gad

385-389

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Metadherin mRNA expression in hepatocellular carcinoma

Nevein M. Al-sheikh, Sally M. El-Hefnway, Ahmed M. Abuamer, Ashraf G. Dala

391-397

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The cephalofacial characterization in humans: The study using igbo tribe in Nigeria

Obaje Godwin Sunday, Uzomba Godwin Chinedu

399-402

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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

Abdollah Gravand, Ali Mohammad Foroughmand, Mehdi Pourmehdi Boroujeni

403-407

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New insights into smudge cell percentage in chronic lymphocytic Leukemia: A novel prognostic indicator of disease burden

Amal Abd El Hamid Mohamed, Nesma Ahmed Safwat

409-415

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Detection of antimicrobial resistance genes of Helicobacter pylori strains to clarithromycin, metronidazole, amoxicillin and tetracycline among Egyptian patients

Manal Diab, Ahmed El-Shenawy, Maged El-Ghannam, Dalia Salem, Moustafa Abdelnasser, Mohamed Shaheen, Mahmoud Abdel-Hady, Effat El-Sherbini, Mohamed Saber

417-423

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Genetic study of the NOTCH3 gene in CADASIL patients

Seyedeh Parisa Chavoshi Tarzjani, Seyed Abolhassan Shahzadeh Fazeli, Mohammad Hossein Sanati, Zahra Mirzayee

425-427

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Cantu syndrome in an Egyptian child

Rabah M. Shawky, Radwa Gamal

429-432

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Asymptomatic hemochromatosis case with HFE c.1007-47G>A, c.340+4T>C heterozygous mutations and alpha globin -3.7 kb deletion

Vesile Deniz Çelik, Betul Orhan Kiliç, Yasemin Ardıçoğlu Akışin, Fatma Ajlan Tükün, Nejat Akar

433-435

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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

Fatma Silan, Romyla Bourouba, Taner Karakaya, Onur Yildiz, Baris Paksoy, Mine Urfali, Ozturk Ozdemir

437-441

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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]

Solaf M. Elsayed, Radwa Gamal

443

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 19 No. 4 (2018) / Articles

Articles

MTHFR C677T polymorphism and risk of esophageal cancer: An updated meta-analysis

Pathophysiology of bleeding diathesis in haemophilia-A: A sequential and critical appraisal of non-FVIII related haemostatic dysfunctions and their therapeutic implications

Helicobacter pylori Western cagA genotype in Egyptian patients with upper gastrointestinal disease

Fuzzy system model for gene expression

Angiotensin-converting enzyme (ACE) I/D and bradykinin B2 receptor T/C genes polymorphism in patients with ACE inhibitors-related cough

Study of DNA methyl transferase 3A mutation in acute myeloid leukemic patients

Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress

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

Pathogenic predictions of non-synonymous variants and their impacts: A computational assessment of ARHGEF6 gene

FLT3 receptor/CD135 expression by flow cytometry in acute myeloid leukemia: Relation to FLT3 gene mutations and mRNA transcripts

Evaluation of health-related quality of life and muscular strength in children with beta thalassemia major

Study of congenital malformations in infants and children in Menoufia governorate, Egypt

In silico analysis of the functional non-synonymous single nucleotide polymorphisms in the human CYP27B1 gene

Renalase gene polymorphisms (rs2576178 and rs10887800) in Egyptian hypertensive end stage renal disease patients

Study of the role of IL-17F gene polymorphism in the development of immune thrombocytopenia among the Egyptian children

Metadherin mRNA expression in hepatocellular carcinoma

The cephalofacial characterization in humans: The study using igbo tribe in Nigeria

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

New insights into smudge cell percentage in chronic lymphocytic Leukemia: A novel prognostic indicator of disease burden

Detection of antimicrobial resistance genes of Helicobacter pylori strains to clarithromycin, metronidazole, amoxicillin and tetracycline among Egyptian patients

Genetic study of the NOTCH3 gene in CADASIL patients

Cantu syndrome in an Egyptian child

Asymptomatic hemochromatosis case with HFE c.1007-47G>A, c.340+4T>C heterozygous mutations and alpha globin -3.7 kb deletion

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

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]

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