Vol. 9 No. 1 (2008) | Egyptian Journal of Medical Human Genetics

Cytomegalovirus in Children

LB El-Din

1-10

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Profile of Egyptian Patients with Mucopolysaccharidosis

RM Shawky, EA Zaki, EM Fateen, MM Refaat, NM Eldin

11-22

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Approaching a Dysmorphic Newborn

SM El-Din, MN Farid, AR Ramy

23-40

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Indicators of Apoptosis in Duchenne Muscular Dystrophy Patients

E Abdel-Salam, L Mansour, I Abdel-Meguid, S Korraa

41-50

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Enzymatic Preparation of Low-Phenylalanine Formula Derived from Skim Milk Hydrolysate for Phenyl ketonuric Patients

AE Shehata, MNI El-Magdoub, TM Kamal, HA Mohamed

51-71

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A Double Blind Study Comparing Virucare and Inter-feron as Treatment for Hepatitis CVirus and its Complications

M El-Aaser, N Omer, HA Hamid, M Hamad, S Omer

71-84

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Sensorineural Hearing Impairment is a Common Feature of Consanguineous Marriage

SMN El-Din, L Hamed

85-92

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Study of Thyroid Function in Children with Attention Deficit Hyperactivity Disorder and Aggressive Behavior

F El Baz, RT Hamza, MAS El-Din, MA Hassan

93-104

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The Impact of Prenatal Diagnosis in Egyptian Families with Duchenne Muscular Dystrophy

LK Effat, KS Amr, AA El-Harouni, KR Gaber

105-110

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Low Incidence of Androgen Receptor Mutation Among Egyptian Children with Androgen Resistance

M Essawi, H Nasr, I Mazen, K Gaafar, K Amr, M Hafez, Y Gad

111-120

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Spotlight on the Diagnosis of Acute Promyelocytic Leukemia (AML-M3) Using Karyotyping, FISH and Quantitative Real-Time PCR

LMF Khudari, FMS Monem

121-130

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 9 No. 1 (2008) / Articles

Articles

Cytomegalovirus in Children

Profile of Egyptian Patients with Mucopolysaccharidosis

Approaching a Dysmorphic Newborn

Indicators of Apoptosis in Duchenne Muscular Dystrophy Patients

Enzymatic Preparation of Low-Phenylalanine Formula Derived from Skim Milk Hydrolysate for Phenyl ketonuric Patients

A Double Blind Study Comparing Virucare and Inter-feron as Treatment for Hepatitis CVirus and its Complications

Sensorineural Hearing Impairment is a Common Feature of Consanguineous Marriage

Study of Thyroid Function in Children with Attention Deficit Hyperactivity Disorder and Aggressive Behavior

The Impact of Prenatal Diagnosis in Egyptian Families with Duchenne Muscular Dystrophy

Low Incidence of Androgen Receptor Mutation Among Egyptian Children with Androgen Resistance

Spotlight on the Diagnosis of Acute Promyelocytic Leukemia (AML-M3) Using Karyotyping, FISH and Quantitative Real-Time PCR

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