نتایج جستجو برای: trisomy of 21

تعداد نتایج: 21198882  

Journal: :American journal of clinical pathology 2000
B Nagy Z Bán E Tóth-Pál C Papp L Fintor Z Papp

Reports documented a higher frequency of apolipoprotein E (apoE) allele epsilon 4 among mothers of children diagnosed with Down syndrome. We studied the prevalence of apoE alleles among 56 conceptuses with trisomy 13, trisomy 18, or trisomy 21. The presence of the 3 most common apoE alleles (epsilon 2, epsilon 3, epsilon 4) was determined by polymerase chain reaction-restriction fragment length...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1993

Journal: :Proceedings of the National Academy of Sciences 2013

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...

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: :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...

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