Vol. 16 No. 4 (2015) | Egyptian Journal of Medical Human Genetics

Moushira Zaki, Shams Kholoussi, Somaia Ismail, Haiam Abdel Raouf, Iman Helwa, Naglaa Hassan, Eman Youness, Nadia A Mohamed, Sanaa Kamal, Walaa Yousef, Mohamed Shaker, Wafaa Ezzat, Yasser A Elhosary, Omnia M Saleh, Mona El Gammal, Hala T El-Bassyouni, Samira Ismail, Mamdouh Bibars, Osama Azmy

367-374

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Effectiveness of sensory integration program in motor skills in children with autism

Amel E Abdel Karim, Amira H Mohammed

375-380

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Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient

Rabah M Shawky, R Gamal, Neveen S Seifeldin

381-385

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A novel nonsense mutation in cathepsin C gene in an Egyptian patient presenting with Papillon–Lefe`vre syndrome

Hala Soliman, Heba Gamal Eldeen, Mustafa Ibrahim Mustafa

387-392

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Letter to the Editor

Nazurah Alwi, Dzalani Harun, JH Leonard

393-394

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 16 No. 4 (2015) / Articles

Articles

The relation between antihistamine medication during early pregnancy & birth defects

An overview on hepatitis C virus genotypes and its control

Radioactive fallout and neural tube defects

Differential response of biochemical parameters to EMS and MMS treatments and their dose effect relationship on chromosomes in induced diabetic mouse

The role of microRNAs on angiogenesis and vascular pressure in preeclampsia: The evidence from systematic review

Lipoprotein lipase gene variants: Association with acute myocardial infarction and lipid profiles

Patatin-like phospholipase domain containing-3 gene (PNPLA3) I148M polymorphism and liver damage in chronic hepatitis C Egyptian patients

Cancer ameliorating potential of Phyllanthus amarus: In vivo and in vitro studies against Aflatoxin B1 toxicity

Rhodopsin mutations are scarcely implicated in autosomal recessive retinitis pigmentosa: A preliminary study of Egyptian retinitis pigmentosa patients

Association of glutathione-S-transferase P1 (GSTP1)-313 A> G gene polymorphism and susceptibility to endometrial hyperplasia among Egyptian women

Metabolic abnormalities in young Egyptian women with polycystic ovary syndrome and their relation to ADIPOQ gene variants and body fat phenotype

Effectiveness of sensory integration program in motor skills in children with autism

Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient

A novel nonsense mutation in cathepsin C gene in an Egyptian patient presenting with Papillon–Lefe`vre syndrome

Letter to the Editor

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