Vol. 13 No. 3 (2012) | Egyptian Journal of Medical Human Genetics

Thalassemia intermedia: An overview

RM Shawky, TM Kamal

245-255

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Association of the UCP2 45-bp insertion/deletion polymorphism with diabetes type 2 and obesity in Saudi population

EH Jiffri

257-262

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The methylenetetrahydrofolate reductase gene variant (C677T) in risk mothers with Down syndrome among Saudi population

MT Tayeb

263-268

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Biofilm formation and presence of icaAD gene in clinical isolates of staphylococci

RA Nasr, HM AbuShady, HS Hussein

269-274

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Homocysteine, folic acid and vitamin B12 levels in serum of epileptic children

ON Eldeen, SH Abd Eldayem, RH Shatla, NA Omara, SS Elgammal

275-280

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Cytogenetic and molecular study in intersex

SS Abou El Ella, MAM Tawfik, DM Ellahony, NM Anees

281-289

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Angiotensin converting enzyme (ACE D/I) polymorphism and its relation to liver fibrosis progression in Egyptian patients with chronic hepatitis C virus infection

AMH Mackawy, MEH Badawy, OAEY Megahed

291-299

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Genotoxic damage in cultured human peripheral blood lymphocytes of oral contraceptive users

F Naz, S Jyoti, N Akhtar, M Afzal, YH Siddique

301-305

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Glutathione S-transferase M1 and T1, CYP1A2-2467T/delT polymorphisms and non small-cell lung cancer risk in Tunisian sample

B Fatma, T Aida, JA Maurice, S Saguem

307-312

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Chromosome 22 microdeletion in children with syndromic congenital heart disease by fluorescent in situ hybridization (FISH)

SSA El-Ella, F El Gendy, MAM Tawfik, E El Sobky, A Khattab, M El-mekkawy

313-322

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Virologic response at week 8 of combined treatment as a predictor of sustained virologic response in non rapid virologic response, chronic HCV genotype 4 infected patients

A Monis, AA Monis, R Al Swaff

331-335

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Hepatoadrenal syndrome in Egyptian children with liver cirrhosis with and without sepsis

AAM Elfaramawy

337-342

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Use of denaturing gradient gel electrophoresis in screening unknown β-thalassemia mutations in Egyptian patients

G Christopoulos, GM Ezzat, M Kleanthous

343-349

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Mitochondrial DNA depletion syndrome presenting with ataxia and external ophthalmoplegia: Case report

L Selim, D Mehaney, F Hassan, R Sabry, R Zeyada, S Hassan, IG Eldin, E Bertini

351-357

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Case Report - Serious life threatening upper airway obstruction in congenital generalized myofibromatosis

RA Abolila, RM Alsawan, HA Masud

359-361

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Case Report - Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst

RA Abolila, RM Alsawan, MT Alrefaie

363-365

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Basic concepts of medical genetics, pathogenetics: Part 1

MSZ Salem

367-370

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 13 No. 3 (2012) / Articles

Articles

Thalassemia intermedia: An overview

Association of the UCP2 45-bp insertion/deletion polymorphism with diabetes type 2 and obesity in Saudi population

The methylenetetrahydrofolate reductase gene variant (C677T) in risk mothers with Down syndrome among Saudi population

Biofilm formation and presence of icaAD gene in clinical isolates of staphylococci

Homocysteine, folic acid and vitamin B12 levels in serum of epileptic children

Cytogenetic and molecular study in intersex

Angiotensin converting enzyme (ACE D/I) polymorphism and its relation to liver fibrosis progression in Egyptian patients with chronic hepatitis C virus infection

Genotoxic damage in cultured human peripheral blood lymphocytes of oral contraceptive users

Glutathione S-transferase M1 and T1, CYP1A2-2467T/delT polymorphisms and non small-cell lung cancer risk in Tunisian sample

Chromosome 22 microdeletion in children with syndromic congenital heart disease by fluorescent in situ hybridization (FISH)

Virologic response at week 8 of combined treatment as a predictor of sustained virologic response in non rapid virologic response, chronic HCV genotype 4 infected patients

Hepatoadrenal syndrome in Egyptian children with liver cirrhosis with and without sepsis

Use of denaturing gradient gel electrophoresis in screening unknown β-thalassemia mutations in Egyptian patients

Mitochondrial DNA depletion syndrome presenting with ataxia and external ophthalmoplegia: Case report

Case Report - Serious life threatening upper airway obstruction in congenital generalized myofibromatosis

Case Report - Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst

Basic concepts of medical genetics, pathogenetics: Part 1

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