نتایج جستجو برای: 21 trisomy

تعداد نتایج: 251021  

Journal: :Annals of Pediatric Cardiology 2014

Journal: :Pediatrics 2015
Tammy Z Movsas Alan R Spitzer Ira H Gewolb

BACKGROUND AND OBJECTIVES Trisomy 21 is known to decrease the risk of several (nonocular) angiogenic-mediated diseases. The objective of this study was to determine whether trisomy 21 can also be shown to be significantly protective against ocular angiogenic-mediated disorders such as retinopathy of prematurity (ROP). METHODS A retrospective analysis of deidentified data from the Pediatrix Ba...

Journal: :Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2015
M M Gil V Accurti B Santacruz M N Plana K H Nicolaides

OBJECTIVE To review clinical validation or implementation studies of maternal blood cell-free (cf) DNA analysis and define the performance of screening for fetal trisomies 21, 18 and 13 and sex chromosome aneuploidies. METHODS Searches of PubMed, EMBASE and The Cochrane Library were performed to identify all peer-reviewed articles on cfDNA testing in screening for aneuploidies between January...

2014
Young Joo Jeon Yulin Zhou Yihan Li Qiwei Guo Jinchun Chen Shengmao Quan Ahong Zhang Hailing Zheng Xingqiang Zhu Jin Lin Huan Xu Ayang Wu Sin-Gi Park Byung Chul Kim Hee Jae Joo Hongliang Chen Jong Bhak Sinuhe Hahn

OBJECTIVE Recent non-invasive prenatal testing (NIPT) technologies are based on next-generation sequencing (NGS). NGS allows rapid and effective clinical diagnoses to be determined with two common sequencing systems: Illumina and Ion Torrent platforms. The majority of NIPT technology is associated with Illumina platform. We investigated whether fetal trisomy 18 and 21 were sensitively and speci...

Journal: :Clinical chemistry 2010
Qiwei Guo Yulin Zhou Xiaobo Wang Qingge Li

BACKGROUND Trisomies 13, 18, and 21 account for the majority of chromosomal aneuploidies detected in prenatal diagnosis. Diagnosis of these trisomies relies mainly on karyotype analysis. Several molecular methods have been developed for trisomy detection, but performance or throughput limitations of these methods currently constrain their use in routine testing. METHODS We developed multiplex...

Journal: :Prenatal diagnosis 2003
Po-Jen Cheng Ching-Ming Liu Ho-Yen Chueh Chien-Ming Lin Yung-Kwei Soong

BACKGROUND Trisomy 18, the second most common autosomal trisomy, has the highest incidence of congenital heart disease of all chromosomal abnormalities. This study assessed the use of nuchal translucency (NT) measurement and fetal echocardiography at 16 to 18 weeks of gestation in prenatal detection for trisomy 18. METHODS Screening for chromosomal aneuploidy using fetal NT measurement was pe...

2012
S. Iliodromiti N. Vrachnis Evangelia Samoli Z. Iliodromiti C. Pangalos N. Drakoulis G. Creatsas D. Botsis

OBJECTIVE We investigated whether the concentration of the glycoprotein fetuin A is altered in the second trimester amniotic fluid of trisomy 21 pregnancies compared with euploid pregnancies. METHODS 25 pregnancies with an extra chromosome 21 were matched for maternal and gestational age with 25 pregnancies with normal karyotype. Levels of fetuin A in amniotic fluid were measured by a commerc...

Journal: :Molecular Cytogenetics 2008

Journal: :International Journal of Disability, Development and Education 2020

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید