The aim of study was to investigate the importance of chromosome aberration in differential diagnosis of eosinophilia and the chromosomal aberrations involved in patients with clonal eosinophilia.
为探讨染色体异常克隆在嗜酸性粒细胞增多症诊断和鉴别诊断中的意义及克隆性嗜酸性粒细胞增多症涉及的染色体异常,收集了65例嗜酸性粒细胞增多患者的骨髓标本,培养24小时,采用G显带进行核型分析。
The chromosomal aberration was checked out in 46 cases from 389 related patients,ratio:11.
其中罗伯逊易位携带者 6例 ,平衡易位携带者10例 ,倒位携带者 4例 ,性染色体异常者 14例 ,先天愚型及发育异常者 12例 。
To investigate chromosomal aberration and HPV18 E6,HPV18 E7 proteins expression in human embryonic esophageal epithelial cells transfected with HPV18 DNA during immortalization and malignant transformation.
[目的 ]研究HPV18DNA转染的人胚食管上皮细胞永生化及其恶性转化过程中的染色体异常和HPV18E6、HPV18E7蛋白表达情况。
The rapid diagnosis of common chromosome abnormality in prenatal diagnosis;
产前诊断中常见染色体异常的快速诊断
This study was to explore the clinical significance of FLT3 internal tandem duplication (FLT3/ITD) in acute myeloid leukemia (AML) with chromosome abnormality.
本研究旨在探讨伴有染色体异常急性髓系白血病患者FLT3跨膜区内部串联重复突变检测的临床意义。
Objective To investigate the frequency of chromosome abnormality in 415 infertile males.
目的研究中国人群男性不育患者的染色体异常频率分布。
Results There were 38 chromosome aberrations(29 women,9 men) in them,the abnormal rate being 3.
结果发现染色体异常核型38例,异常发生率为3。
Relationship between fetal abnormal ultrasound examination and fetal abnormal karyotype in pregnancy
妊娠期胎儿超声筛查异常与胎儿染色体异常的关系探讨
Diagnosis of Fetal Chromosomal Abnormalities via Amniocentesis:Analysis of 2355 Cases
羊膜腔穿刺2355例诊断胎儿染色体异常的分析
Progress of the Ultrasonographic Diagnosis of Miniabnormalities Caused by Chromosomal Abnormalities
胎儿染色体异常相关的微小畸形超声诊断进展
The Value of Prenatal Diagnosis Indication in the Diagnosis of Fetal Chromosomal Abnormalities
产前诊断指征在胎儿染色体异常诊断中的价值探讨
Analysis of Ultrasonographic Examination in Fetuses with Chromosome Karyotype Abnormalities
染色体核型异常胎儿的超声检查分析
The relationship between abnormal chromosome of fetal cord blood and abnormal changes of ultrasound
胎儿脐血染色体异常与超声异常改变的相关性
The significance of ultrasound in prenatal diagnosis of chromosome abnormality
超声在染色体异常胎儿产前诊断中的意义
Morphological Characteristics Study and Prenatal Diagnosis On Chromosomal Abnormal Fetus
染色体异常胎儿的畸形形态学特征与产前诊断
Application research of multiplex ligation-dependent probe amplification (MLPA) in rapid prenatal detection of aneuploid abnormalities
MLPA技术在快速检测胎儿染色体非整倍体异常中的应用
The relationship between prenatal ultrasongraphy of fetal choroid plexus cysts and abnormal chromosome
产前超声检查胎儿脉络丛囊肿与染色体异常的关系
To evaluate the feasibility of using FISH for the detection of fetal chromosomal abnormalities
荧光原位杂交技术在检测胎儿染色体数目异常中的应用
Clinical value of prenatal ultrasound screening for fetal malformation due to chromosomal abnormalities
产前超声筛查染色体异常所致胎儿畸形的临床价值
Meta-analysis of screening for chromosomal abnormalities using elevated nuchal translucency in first trimester
孕早期胎儿颈项透明层增厚对染色体异常产前筛查价值的Meta分析
The Chromosomal Constitution of Human Abnormal Zygotes and Embryos
人类异常受精卵及胚胎的染色体组成
Preimplantation Genetic Diagnosis for Patients with Chromosome Structure Abnormalities;
染色体异常者的胚胎植入前遗传学诊断研究
The Relationship of APC and EB1 Gene Expresions with Chromosome Number Abnormity Embryo;
APC和EB1基因表达与染色体数目异常胚胎关系
Noninvasive Prenatal Diagnosis of Chromosome Aneuploidies Using Fetal Nucleated Erythrocytes Circulating in Maternal Peripheral Blood;
利用孕妇外周血中胎儿有核红细胞无创性产前诊断染色体非整倍体异常
Emb ryos were divided into normal and abn ormal chromosome group. Among 67embryos,16were normal and 51were abnormal.
【结果】分析的67个胚胎中,染色体正常16个,异常51个。
