Vol. 16 No. 2 (2015) | Egyptian Journal of Medical Human Genetics

Formal genetic maps

MSZ Salem

101-116

download PDF

SIRT1 gene is associated with cardiovascular disease in the Iranian population

N Mohtavinejad, A Nakhaee, H Harati, J Poodineh, M Afzali

117-122

download PDF

XmnI polymorphism: Relation to β-thalassemia phenotype and genotype in Egyptian Children

F Said, A Abdel-Salam

123-127

download PDF

Study of the effect of HFE gene mutations on iron overload in Egyptian thalassemia patients

MM Wilson, H Al-Wakeel, F Said, M El-Ghamrawy, M Assaad, A El-Beshlawy

129-133

download PDF

The population structure of Ukraine in relation to the phenylthiocarbamide sensitivity

OV Filiptsova, IA Timoshyna, YN Kobets, MN Kobets, IS Burlaka, IA Hurko

135-139

download PDF

Comparative frequency and allelic distribution of ABO and Rh (D) blood groups of major tribal communities of southern Bangladesh with general population and their determinants

G Dewan

141-147

download PDF

Multidisciplinary approach for evaluation of neurocutaneous disorders in children in Sohag University Hospital, Upper Egypt

AA Sadek, SN Abdel-Samad, MA Bakheet, IAA Hassan, WM Abd El Mageed, AM Emam

149-157

download PDF

Prenatal genetic testing, counseling and follow-up of 33 Egyptian pregnant females with history of mucopolysaccharidoses

KR Gaber, MM Ibrahim, MK Farag, ZY Abdallah, SH Eldessouky, EM Fateen

159-163

download PDF

Selective screening in neonates suspected to have inborn errors of metabolism

RM Shawky, HS Abd-El Khalek, SE Elakhdar

165-171

download PDF

Integrated effect of treadmill training combined with dynamic ankle foot orthosis on balance in children with hemiplegic cerebral palsy

AEAA Sherief, AAA Gazya, MAA El Gafaar

173-179

download PDF

Bicycle ergometer versus treadmill on balance and gait parameters in children with hemophilia

RA Mohamed, AEAA Sherief

181-187

download PDF

Berardinelli–Seip syndrome type 2 – An Egyptian child

RM Shawky, R Gamal, NS Seifeldin

189-193

download PDF

Absent abdominal muscles, nephro-urologic abnormalities, and severe neurologic damage in an infant with 3 chromosomal duplications: A novel syndrome?

KF Akl, JH Albaramki, EA Ghani, MA Al Qaisi, N Abujaber, P Tavares

195-197

download PDF

Co-occurrence of Xp21 microduplication encompassing the DMD locus in conjunction with 17p12/PMP22 microduplication in a female with Charcot–Marie–Tooth disease type 1A

A Sidhu, M Hankerd, K Kennelly, M Kristofice, S Ebrahim

199-204

download PDF

Letter to the Editor

M Saadat

205-206

download PDF

Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 16 No. 2 (2015) / Articles

Articles

Formal genetic maps

SIRT1 gene is associated with cardiovascular disease in the Iranian population

XmnI polymorphism: Relation to β-thalassemia phenotype and genotype in Egyptian Children

Study of the effect of HFE gene mutations on iron overload in Egyptian thalassemia patients

The population structure of Ukraine in relation to the phenylthiocarbamide sensitivity

Comparative frequency and allelic distribution of ABO and Rh (D) blood groups of major tribal communities of southern Bangladesh with general population and their determinants

Multidisciplinary approach for evaluation of neurocutaneous disorders in children in Sohag University Hospital, Upper Egypt

Prenatal genetic testing, counseling and follow-up of 33 Egyptian pregnant females with history of mucopolysaccharidoses

Selective screening in neonates suspected to have inborn errors of metabolism

Integrated effect of treadmill training combined with dynamic ankle foot orthosis on balance in children with hemiplegic cerebral palsy

Bicycle ergometer versus treadmill on balance and gait parameters in children with hemophilia

Berardinelli–Seip syndrome type 2 – An Egyptian child

Absent abdominal muscles, nephro-urologic abnormalities, and severe neurologic damage in an infant with 3 chromosomal duplications: A novel syndrome?

Co-occurrence of Xp21 microduplication encompassing the DMD locus in conjunction with 17p12/PMP22 microduplication in a female with Charcot–Marie–Tooth disease type 1A

Letter to the Editor

Journal Identifiers