نتایج جستجو برای: hbbarts.

تعداد نتایج: 4  

Journal: :Clinical chemistry 2007
Sherry Sze Yee Ho Samuel S Chong Evelyn S C Koay Yiong Huak Chan Ponnusamy Sukumar Lily-Lily Chiu Wen Wang Ashim Roy Mary Rauff Lin Lin Su Arijit Biswas Mahesh Choolani

BACKGROUND We sought to develop a rapid prenatal diagnostic test for simultaneous detection of HbBarts hydrops fetalis and exclusion of maternal contamination. METHODS We developed a multiplex quantitative fluorescent PCR (QF-PCR) test that detects the presence/ absence of 2 microsatellite markers (16PTEL05/16PTEL06) located within breakpoints of the Southeast Asia ((-SEA)) deletion. HbBarts ...

Journal: :medical journal of islamic republic of iran 0
nasrin khalesi pediatrics department, faculty of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) nastaran khosravi pediatrics department, faculty of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) mohammad reza rezaee faculty of medicine, tehran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) leila amini midwifery department, faculty of nursing & midwifery, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

background :identification of α thalassemia (α thal) a common cause of microcytosis during neonatal periods is an important step prevent unnecessary interventions. thus, low the mean corpuscular volume (mcv) and the mean corpuscular hemoglobin (mch) may consider as α-thalassemia key detection points. the present study aimed to determine the prevalence of microcytosis among neonates who born in ...

Journal: :Clinical chemistry 1992
F P van der Dijs G A van den Berg J G Schermer F D Muskiet H Landman F A Muskiet

We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genotype frequencies of the structural hemoglobin variants HbS and HbC and the synthesis variants alpha- and beta(+)-thalassemia in babies born on Curaçao. During three months, 67.2% of all (748) newborns were screened: 122 (24.3%) had an abnormal hemoglobin pattern, of which 53 (43.4%) had a hemoglob...

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