Vol. 9 No. 2 (2008) | Egyptian Journal of Medical Human Genetics

Cholestasis in neonates and infants

A Elfaramawy

135-147

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Haemochromatosis gene mutation H63D is a risk factor for iron overload in Egyptian beta- thalassemic children

FH El-Rashidi, AE Elshafey, SM Ragab, FF Hegazy, SEH El-Nabi

149-160

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Craniofacial proportions and anthropometric measurements among growth hormone deficient Egyptian children

M Rashad, N Amr, ME Badwy, H Elsedfy

161-170

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Genetic evaluation of proportionate short stature in Alexandria, Egypt

AK Behery

171-180

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Cytokines and growth factors in Duchene muscular dystrophy patients

I Abdel-Megui, E Abdel-Salam, S Korraa

181-188

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Phenotypic variability in patients with isodicentric Y(p11.3). a clinical, cytogenetic and molecular study

NA Nazmy, SF Kholeif, AK Behery

189-200

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Paraoxonase 1 activity and genotyping in systemic lupus erythematosus and their relationships with cardiovascular complications

HA Abdel-Azeez, S Sharaf, AA Emerah, SA Shoeib

201-214

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Developmental abnormalities of mid and hindbrain: A study of 23 Egyptian patients

LA Selim, MS Zaki, HA Hussein, SN Saleem, AS Kotoury, MY Issa

215-236

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Frequency of fragile-x in x‑linked mental retardation

ES El Sobky, SA El‑Ella, MA Tawfik, WF Mohamed

237-248

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Holoprosencephaly:a report of 2 cases with different presentations

RM Shawky, DI Sadik

249-256

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C syndrome in an Egyptian infant with dilated brain ventricles and heteroto pia

RM Shawky, DI Sadik

257-262

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 9 No. 2 (2008) / Articles

Articles

Cholestasis in neonates and infants

Haemochromatosis gene mutation H63D is a risk factor for iron overload in Egyptian beta- thalassemic children

Craniofacial proportions and anthropometric measurements among growth hormone deficient Egyptian children

Genetic evaluation of proportionate short stature in Alexandria, Egypt

Cytokines and growth factors in Duchene muscular dystrophy patients

Phenotypic variability in patients with isodicentric Y(p11.3). a clinical, cytogenetic and molecular study

Paraoxonase 1 activity and genotyping in systemic lupus erythematosus and their relationships with cardiovascular complications

Developmental abnormalities of mid and hindbrain: A study of 23 Egyptian patients

Frequency of fragile-x in x‑linked mental retardation

Holoprosencephaly:a report of 2 cases with different presentations

C syndrome in an Egyptian infant with dilated brain ventricles and heteroto pia

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