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538  Articles
1 of 55 pages  |  10  records  |  more records»
 
Haemoglobin H (Hb H) disease presented as moderate to severe anaemia and commonly occurs in the form of deletional Hb H. An eleven years old, Chinese girl and her mother’s (a Papua New Guinea ethnicity) samples were referred to Institute for Med... see more

Introduction: Children with DiGeorge syndrome/chromosome 22q11.2 deletion syndrome might have a variable degree of immunodeficiency, which may limit the use of live vaccines. The aim of this study was to review the adverse effects of live vaccines an... see more

The present paper investigates the Hijazi Arabic (HA) morphosyntactic properties of the widely known linguistic phenomenon of sluicing from a generative perspective, taking into account the latest advancements of the Minimalist Approach (Chomsky 1995, 200... see more

The purpose of this study is to investigate the linguistic phenomenon of Acoustic Prepositional Deletion (APD) ( ??? ?????? ?????? , naz?i al-khafi? sma?yan) in the Quran. It mainly addresses deleting thepreposition ??? , ila from some verses of the Quran... see more

BACKGROUND: Glutathione S-transferase (GST), together with other drug-metabolizing enzymes (N-acetyltransferase and cytochrome P450), plays a crucial role in the metabolism of isoniazid (isonicotinic acid hydrazide). Among five isoforms of GST, GSTM1, and... see more

Duplications of 1q concomitant with other chromosomal deletions are rare conditions in association with compound phenotypes. We present a case with a duplication of 1q42.13-q44 and a deletion at 14q32.33 and perform a comprehensive review on relevant case... see more

We report on a newborn female infant with a unique ring chromosome 13. Prenatal findings include intrauterine growth restriction (IUGR); ventricular septal defect (VSD), overriding aorta, and pulmonary stenosis. Postnatal examination found mild dysmorphic... see more

We report on a newborn female infant with a unique ring chromosome 13. Prenatal findings include intrauterine growth restriction (IUGR); ventricular septal defect (VSD), overriding aorta, and pulmonary stenosis. Postnatal examination found mild dysmorphic... see more

Background Renin Angiotensin Aldosteron System plays major role in hypertension pathophysiology. Has been proposed that half of individuals with essential hypertension are considered insulin resistant. Angiotensin Converting Enzyme gene polymorphism takin... see more

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