Vol. 15 No. 4 (2014) | Egyptian Journal of Medical Human Genetics

Published: 2014-10-23

Editorial Board

R M Shawky

iii-iv

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Review: The scope of clinical morbidity in sickle cell trait

A A Tantawy

319-326

DOI:

10.1016/j.ejmhg.2014.08.008

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Chemopreventive effect of Annona muricata on DMBA-induced cell proliferation in the breast tissues of female albino mice

J B Minari

327-334

DOI:

10.1016/j.ejmhg.2014.05.001

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Study of genotype–phenotype correlation of methylene tetrahydrofolate reductase (MTHFR) gene polymorphisms in a sample of Egyptian autistic children

R M Shawky, F El-baz, T M Kamal, R M Elhossiny, M A Ahmed, G H El Nady

335-341

DOI:

10.1016/j.ejmhg.2014.05.004

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Evaluation of chromosomal aberrations induced by hydralazine in Chinese hamster ovary cells

M Sedigh-Ardekani, M Saadat

343-346

DOI:

10.1016/j.ejmhg.2014.06.002

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Heritability of fear: Ukrainian experience

O V Filiptsova, L A Atramentova, Y N Kobets

347-353

DOI:

10.1016/j.ejmhg.2014.07.001

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Association of insertion–deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients

O M Hassanin, M Moustafa, T M El Masry

355-360

DOI:

10.1016/j.ejmhg.2014.06.001

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Soluble receptor for advanced glycation end products (sRAGE) and carotid intima-media thickness (CIMT) in type 1 diabetes Mellitus: Possible association with diabetic vascular complications

E M Sherif, A A Abdelmaksoud, H M Issa, S A Mohamed

361-367

DOI:

10.1016/j.ejmhg.2014.06.003

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Subclinical renal abnormalities in young thalassemia major and intermedia patients and its relation to chelation therapy

A A Adly, D N Toaima, N S Mohamed, K M El Seoud

369-377

DOI:

10.1016/j.ejmhg.2014.06.004

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Fifteen years experience: Egyptian metabolic lab

E M Fateen, M S Ibrahim, Z Y Abdallah

379-385

DOI:

10.1016/j.ejmhg.2014.07.002

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Study of toll-like receptor 7 expression and interferon α in Egyptian patients with chronic hepatitis C Infection and Hepatocellular Carcinoma

T A Abdel-Raouf, A Ahmed, W K Zaki, H M Abdella, M A Zid

387-392

DOI:

10.1016/j.ejmhg.2014.07.003

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Case Report: Meier-Gorlin syndrome: Report of an additional patient with congenital heart disease

R M Shawky, H S Abd-Elkhalek Elabd, R Gamal, S A Mohammad, S Gad

393-398

DOI:

10.1016/j.ejmhg.2014.04.003

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Case Report: Oral–Facial–Digital Syndrome type VI with self mutilations

R M Shawky, H S Abd-Elkhalek Elabd, S Gad, R Gamal, S A Mohammad

399-403

DOI:

10.1016/j.ejmhg.2014.05.006

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Letter to the Editor:Hardy–Weinberg equilibrium and association study of insertion/deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients

M Saadat

405-406

DOI:

10.1016/j.ejmhg.2014.07.004

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Editorial: Subclinical hypothyroidism in children with Down syndrome: To treat or not to treat???

S M Elsayed

407-408

DOI:

10.1016/j.ejmhg.2014.08.003

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Educational Corner of the Issue: Basic concepts of medical genetics. Formal genetics, part 4

M S Salem

409-415

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 15 No. 4 (2014) / Articles

Articles

Editorial Board

Review: The scope of clinical morbidity in sickle cell trait

DOI:

Chemopreventive effect of Annona muricata on DMBA-induced cell proliferation in the breast tissues of female albino mice

DOI:

Study of genotype–phenotype correlation of methylene tetrahydrofolate reductase (MTHFR) gene polymorphisms in a sample of Egyptian autistic children

DOI:

Evaluation of chromosomal aberrations induced by hydralazine in Chinese hamster ovary cells

DOI:

Heritability of fear: Ukrainian experience

DOI:

Association of insertion–deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients

DOI:

Soluble receptor for advanced glycation end products (sRAGE) and carotid intima-media thickness (CIMT) in type 1 diabetes Mellitus: Possible association with diabetic vascular complications

DOI:

Subclinical renal abnormalities in young thalassemia major and intermedia patients and its relation to chelation therapy

DOI:

Fifteen years experience: Egyptian metabolic lab

DOI:

Study of toll-like receptor 7 expression and interferon α in Egyptian patients with chronic hepatitis C Infection and Hepatocellular Carcinoma

DOI:

Case Report: Meier-Gorlin syndrome: Report of an additional patient with congenital heart disease

DOI:

Case Report: Oral–Facial–Digital Syndrome type VI with self mutilations

DOI:

Letter to the Editor:Hardy–Weinberg equilibrium and association study of insertion/deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients

DOI:

Editorial: Subclinical hypothyroidism in children with Down syndrome: To treat or not to treat???

DOI:

Educational Corner of the Issue: Basic concepts of medical genetics. Formal genetics, part 4

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