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Issue Title
Vol 18, No 3 (2017) Molecular genetic analysis of Type II diabetes associated m.3243A>G mitochondrial DNA mutation in a Pakistani family Abstract   PDF
Saidul Abrar, Khushi Muhammad, Hasnain Zaman, Suleman Khan, Faisal Nouroz, Nousheen Bibi
Vol 11, No 2 (2010) Molecular genetics of hemophilia A: Clinical perspectives Abstract   PDF
AAG Tantawy
Vol 16, No 3 (2015) Molecular study of developmental sex disorders in children Abstract   PDF
SS AboElella, MAM Tawfik, WMM Abo El-Fotoh
Vol 19, No 4 (2018) MTHFR C677T polymorphism and risk of esophageal cancer: An updated meta-analysis Abstract   PDF
Pradeep Kumar, Vandana Rai
Vol 16, No 2 (2015) Multidisciplinary approach for evaluation of neurocutaneous disorders in children in Sohag University Hospital, Upper Egypt Abstract   PDF
AA Sadek, SN Abdel-Samad, MA Bakheet, IAA Hassan, WM Abd El Mageed, AM Emam
Vol 14, No 1 (2013) Multiple molecular markers MAGE-1, MAGE-3 and AFP mRNAs expression nested PCR assay for sensitive and specific detection of circulating hepatoma cells: Enhanced detection of hepatocellular carcinoma Abstract   PDF
SH Teama, SHA Agwa, NA ElNakeeb, MA Hamid, AM Maher, MM Heidar
Vol 19, No 2 (2018) Multiplex polymerase chain reaction: Could change diagnosis of Ventilator-associated pneumonia in pediatric critical care units to the fast track? Abstract   PDF
Mervat Gamal Eldin Mansour, Sherin Albendary
Vol 8, No 2 (2007) MURCS association: a case report Abstract   PDF
RM Shawky, IM Talaat, ZI El-Hakim, SM Elsayed
Vol 18, No 3 (2017) Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases Abstract   PDF
Solaf M. Elsayed, Nagia Fahmy, Radwa Gamal, Mohamed Wafik, Dina Zamzam, Mai Fahmy, Mahmoud Suelam
Vol 19, No 4 (2018) New insights into smudge cell percentage in chronic lymphocytic Leukemia: A novel prognostic indicator of disease burden Abstract   PDF
Amal Abd El Hamid Mohamed, Nesma Ahmed Safwat
Vol 19, No 3 (2018) No association between the SNP rs1625579 in miR-137 gene and schizophrenia in Iranian population Abstract   PDF
Azadeh Abtahi, Nader Mansour Samaei, Naghmeh Gholipour, Noorodin Moradi
Vol 12, No 1 (2011) Non HLA genetic markers association with type-1 diabetes mellitus Abstract   PDF
SSA El-Ella, AA Shaltout, MAM Tawfik, M Deeb, DM EL-Lahony, ES Khatab, NF Barseem
Vol 18, No 1 (2017) Non‐invasive prenatal screening for chromosomal abnormalities using circulating cell-free fetal DNA in maternal plasma: Current applications, limitations and prospects Abstract   PDF
Cláudia Amorim Costa
Vol 15, No 3 (2014) Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy Abstract   PDF
R M Shawky, S M Elsayed, T Todorov, A Zibert, S Alawbathani, H J Schmidt
Vol 14, No 1 (2013) Non-HLA gene polymorphisms and their implications on dengue virus infection Abstract   PDF
H Harapan, JK Fajar, N Wahyuniati, JR Anand, L Nambaru, KF Jamil
Vol 14, No 2 (2013) Novel mutation predicted to disrupt SGOL1 protein function Abstract   PDF
Rohit Gupta, Mrinal Mishra, Prateek Tandon, Raunak Hisaria
Vol 18, No 2 (2017) NUCB2/Nesfatin-1: A Potent Meal Regulatory Hormone and its Role in Diabetes Abstract   PDF
Soodabeh Khalili, Mahmoud Shekari Khaniani, Fatemeh Afkhami, Sima Mansoori Derakhshan
Vol 18, No 1 (2017) Null association of maternal MTHFR A1298C polymorphism with Down syndrome pregnancy: An updated meta-analysis Abstract   PDF
Vandana Rai, Upendra Yadav, Pradeep Kumar
Vol 12, No 2 (2011) Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population Abstract   PDF
NA Elhawary, N Bogari, M Rashad, MT Tayeb
Vol 12, No 1 (2011) Nutritional genomics and personalized diet Abstract   PDF
NEA Gaboon
Vol 16, No 3 (2015) Occurrence and detection of AmpC β-lactamases among Enterobacteriaceae isolates from patients at Ain Shams University Hospital Abstract   PDF
SA El-Hady, LA Adel
Vol 12, No 2 (2011) Ocular features in Egyptian genetically disabled children Abstract   PDF
GR El-Hawary, RM Shawky, AS El-Din, SMN El-Din
Vol 10, No 1 (2009) One gene, many phenotypes Abstract   PDF
RM Shawky
Vol 18, No 4 (2017) Open-array analysis of genetic variants in Egyptian patients with type 2 diabetes and obesity Abstract   PDF
Hanaa R.M. Attia, Solaf A. Kamel, Mona H. Ibrahim, Heba A. Farouk, Amany H.A. Rahman, Ghada H. Sayed, Nevine I. Musa
Vol 17, No 1 (2016) Opitz C syndrome: Trigonocephaly, mental retardation and craniofacial dysmorphism Abstract   PDF
J.A. Avina Fierro, D.A. Hernandez Avina
Vol 14, No 3 (2013) Oral-facial-digital syndrome type II: Transitional type between Mohr and Varadi Abstract   PDF
RM Shawky, SM Elsayed, HS Abd-Elkhalek, S Gad
Vol 15, No 3 (2014) Oral-facial-digital syndrome with mesoaxial polysyndactyly, common AV canal, hirschsprung disease and sacral dysgenesis: Probably a transitional type between II, VI, variant of type VI or a new type Abstract   PDF
R M Shawky, H S Abd Elkhalek, M M Al-Fahham, S A Mohammad, S Gad
Vol 9, No 2 (2008) Paraoxonase 1 activity and genotyping in systemic lupus erythematosus and their relationships with cardiovascular complications Abstract   PDF
HA Abdel-Azeez, S Sharaf, AA Emerah, SA Shoeib
Vol 18, No 1 (2017) Parathyroid hormone in pediatric patients with β-thalassemia major and its relation to bone mineral density; a case control study Abstract   PDF
Mostafa El-Nashar, Ahmed Kamel Mortagy, Nagham M.S. El-Beblawy, Eman El-Gohary, Irene Mokhtar Kamel, Mona Rashad, Wessam A. Mouharam
Vol 17, No 2 (2016) Partial association of restriction polymorphism of the ligand binding domain of human androgen receptor in prostate cancer Abstract   PDF
Mohamed Hessien, Ahmed El Barbary, Saad el Gendy, Amira Nabil
Vol 8, No 2 (2007) Partial duplication of chromosome 8p: Report of 5 patients and review of literature Abstract   PDF
MJ Marafie, MM Abu-Henedi, SJ Abulhasan, A Al-Wadaani
Vol 16, No 4 (2015) Patatin-like phospholipase domain containing-3 gene (PNPLA3) I148M polymorphism and liver damage in chronic hepatitis C Egyptian patients Abstract   PDF
Amal MH Mackawy, Mohamed EH Badawi, Ola Megahed
Vol 17, No 1 (2016) Pathogenetics. An introductory review Abstract   PDF
Mohammad Saad Zaghloul Salem
Vol 19, No 4 (2018) Pathogenic predictions of non-synonymous variants and their impacts: A computational assessment of ARHGEF6 gene Abstract   PDF
Yashvant M. Khimsuriya, Jenabhai B. Chauhan
Vol 19, No 4 (2018) Pathophysiology of bleeding diathesis in haemophilia-A: A sequential and critical appraisal of non-FVIII related haemostatic dysfunctions and their therapeutic implications Abstract   PDF
Umma A. Ibrahim, Sagir G. Ahmed
Vol 11, No 1 (2010) Peters’ plus syndrome in an Egyptian patient with some unusual features Abstract   PDF
R Shawky, HS Abd-Elkhalek
Vol 17, No 3 (2016) Phenotypic and molecular genetic analysis of Pyruvate Kinase deficiency in a Tunisian family Abstract   PDF
Jaouani Mouna, Hamdi Nadia, Chaouch Leila, Kalai Miniar, Mellouli Fethi, Darragi Imen, Boudriga Imen, Chaouachi Dorra, Bejaoui Mohamed, Abbes Salem
Vol 9, No 2 (2008) Phenotypic variability in patients with isodicentric Y(p11.3). a clinical, cytogenetic and molecular study Abstract   PDF
NA Nazmy, SF Kholeif, AK Behery
Vol 13, No 1 (2012) Phototherapy and DNA changes in full term neonates with hyperbilirubinemia Abstract   PDF
MYZ El-Abdin, MA El-Salam, MY Ibrhim, SSM Koraa, E Mahmoud
Vol 13, No 1 (2012) Pilot study for assessment of prevalence of intrafamilial hepatitis C transmission in relation to salivary viral load among infected patients with and without chronic renal failure Abstract   PDF
H El Tayeb, NA El Nakeeb, MM Sayed, WA Yousry, SHA Agwa
Vol 17, No 1 (2016) Pilot study for early prognosis of Azoospermia in relation to Y-STR Profiling Abstract   PDF
Ahmed M. Refaat
Vol 16, No 3 (2015) Plummer Vinson syndrome in a male and his chromosomal study – A case report Abstract   PDF
SK Swain, R Panigrahy, MC Sahu
Vol 17, No 3 (2016) Polymorphism in leptin receptor gene was associated with obesity in Yogyakarta, Indonesia Abstract   PDF
Pramudji Hastuti, Izza Zukhrufia, Made Harumi Padwaswari, Afifah Nuraini, Ahmad Hamim Sadewa
Vol 12, No 1 (2011) Porphyrins profile by high performance liquid chromatography/electrospray ionization tandem mass spectrometry for the diagnosis of porphyria Abstract   PDF
E Fateen, A Abd-Elfattah, L Ragab, W Nazim
Vol 14, No 3 (2013) Possible association of interleukin-1beta (-511C/T) and interleukin-6 (-174G/C) gene polymorphisms with atherosclerosis in end stage renal disease Egyptian patients on maintenance haemodialysis Abstract   PDF
MH Kandil, GM Magour, GI Khalil, DA Maharem, AM Nomair
Vol 10, No 1 (2009) Prenatal diagnosis of aneuploidy among a sample of Egyptian high risk pregnancies Abstract   PDF
RM Shawky, EA Zaky, ES El-Sobky, AR Ramy, SY Omer
Vol 16, No 2 (2015) Prenatal genetic testing, counseling and follow-up of 33 Egyptian pregnant females with history of mucopolysaccharidoses Abstract   PDF
KR Gaber, MM Ibrahim, MK Farag, ZY Abdallah, SH Eldessouky, EM Fateen
Vol 14, No 4 (2013) Prenatal genotyping of Gaucher disease in Egypt Abstract   PDF
S Elgawhary, HA Ghaffar, K Eid, MA Wahab, WS Ragab, WF Saleh
Vol 13, No 2 (2012) Prevalence and clinical significance of anti-C1q antibodies in cutaneous and systemic lupus erythematosus Abstract   PDF
A Hegazy, AF Barakat, MA El Gayyar, LF Arafa
Vol 14, No 1 (2013) Prevalence and gene frequencies of A1A2BO and Rh(D) blood group alleles among some Muslim populations of North India Abstract   PDF
R Hussain, M Fareed, A Shah, M Afzal
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ISSN: 1110-8630
AJOL African Journals Online