Use of Allele-Specific-Amplification Refractory Mutation System–Polymerase Chain Reaction for the Detection of Thyroid-Stimulating Hormone Receptor Gene Mutation in an Indian Fam

The Frequency, Types and Risk Factors of Congenital Anomalies in a Tertiary Neonatal Intensive Care Unit (A hospital based study)

Newborn Screening for Congenital Hypothyroidism and Congenital Adrenal Hyperplasia in Egypt

Determination of Neopterin and Biopterin in Dried Blood Spot by Tandem Mass Spectrometry in Classic and Atypical Hyperphenylalaninemia

Newborn Screening for Certain Treatable Inborn Errors of Metabolism in Alexandria

SCREENING OF EGYPTIAN PATEINTS SUFFERING FROM INBORN AMINO ACID METABOLIC DISORDERS

Cord Blood Hemoglobin A1c and MCP-1 as Predictors for Cardiomyopathy in Infants of Mothers with Gestational Diabetes

Associated Cardiac Anomalies Detected by Echocardiography in Infants and Children with Congenital Malformations. A Prospective-Analytical Study

Screening For Very Long Chain Fatty Acids in Egyptian Children with Inherited Peroxisomal Disorders

Screening of inborn errors of metabolism among Egyptian pediatric intensive care unit (PICU) patients by tandem mass spectrometry