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

Published: 2012-10-05

Thalassemia intermedia: An overview

RM Shawky, TM Kamal

245-255

DOI:

10.1016/j.ejmhg.2012.03.006

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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

DOI:

10.1016/j.ejmhg.2012.04.002

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

MT Tayeb

263-268

DOI:

10.1016/j.ejmhg.2012.04.003

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

RA Nasr, HM AbuShady, HS Hussein

269-274

DOI:

10.1016/j.ejmhg.2012.04.007

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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

DOI:

10.1016/j.ejmhg.2012.05.002

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Cytogenetic and molecular study in intersex

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

281-289

DOI:

10.1016/j.ejmhg.2012.06.003

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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

DOI:

10.1016/j.ejmhg.2012.06.006

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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

DOI:

10.1016/j.ejmhg.2012.06.002

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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

DOI:

10.1016/j.ejmhg.2012.05.001

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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

DOI:

10.1016/j.ejmhg.2012.04.006

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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

DOI:

10.1016/j.ejmhg.2012.03.002

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

AAM Elfaramawy

337-342

DOI:

10.1016/j.ejmhg.2012.04.005

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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

DOI:

10.1016/j.ejmhg.2012.06.008

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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

DOI:

10.1016/j.ejmhg.2012.05.003

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

RA Abolila, RM Alsawan, HA Masud

359-361

DOI:

10.1016/j.ejmhg.2012.06.004

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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

DOI:

10.1016/j.ejmhg.2012.06.005

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Basic concepts of medical genetics, pathogenetics: Part 1

MSZ Salem

367-370

DOI:

10.1016/j.ejmhg.2012.07.001

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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

DOI:

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

DOI:

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

DOI:

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

DOI:

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

DOI:

Cytogenetic and molecular study in intersex

DOI:

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

DOI:

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

DOI:

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

DOI:

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

DOI:

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

DOI:

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

DOI:

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

DOI:

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

DOI:

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

DOI:

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

DOI:

Basic concepts of medical genetics, pathogenetics: Part 1

DOI:

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