Trisomy

The observation of human colon cancer cells with chromosome trisomy 7 after culture in vitro

人大肠癌细胞体外培养后的染色体三体性-7观察

Trisomy of Chromosome 8 of a Transplantation of Lymphocytic Leukemia L_ ( 7212 ) in Mice

小鼠可移植性淋巴细胞性白血病L（7212）8号染色体三体性研究

A Method for Rapid and Early Diagnosis of Trisomy 21 Using Molecular Techniques

DNA分析法快速诊断21三体综合征

FISH detected 1 case with trisomy 8 among 50 cases .

FISH分析50例患者中1例+8。

Establishment of a human embryonic stem cell line with trisomy 16

染色体16三体人胚胎干细胞系的建立

A case of X - trisomy and its genetic analysis

X三体型一例及其遗传分析

Prenatal diagnosis for trisomy 18 & analysis of 9 cases

9例18三体综合征胎儿的产前诊断

The practical value with antenatal filtering examination to diagnosis trisomy syndrome

产前筛查在诊断18-三体综合征中的应用价值

Epidemiological investigation and analysis on the risk factors of 108 cases with 21 trisomy syndrome

108例21三体综合征患儿危险因素分析

Objective To establish a method of fluorescence quantitative PCR to detect 21 trisomy syndrome .

目的建立荧光定量PCR技术检测21三体综合征。

Prenatal diagnosis of 21 trisomy syndrome by fluorescence quantitative polymerase chain reaction

应用荧光定量PCR产前诊断21三体综合征

Analysis of trisomy of chromosome 21 syndrome of 376 cases heredity consultants

广东部分地区376例遗传咨询者染色体21-三体综合征分析

Clinical Analysis of Ultrasound Abnormality in Fetuses with Trisomy 18

18-三体综合征胎儿超声异常临床分析

Cerebral CT Manifestations of 21 Trisomy Syndrome in Children

小儿21三体综合征的脑部CT表现

Significance of prenatal ultrasonography in diagnosis of trisomy 18 syndrome

超声在18-三体综合征产前诊断中的意义

Preclinical Study of Preimplantation Genetic Diagnosis of 21 Trisomy Syndrome

21三体综合症植入前诊断的临床前运用研究

Isolate trisomy 8 ( 21 cases ) was the most common numerical abnormality .

单纯+8（21例）为常见的数目异常。

Trisomy has been the focus of extensive medical research but the exact mechanism is still not understood .

三体综合症在医学研究上备受关注，但其确切机制仍未明确。

Inv ( 16 ) was positive in all three cases with trisomy 22 FISH analysis .

3例+22患者FISH检测inv（16）均阳性。

Objective : To improve the understanding and diagnostic ability of the brain changes in21 trisomy syndrome .

目的：提高对小儿21三体综合征脑部CT表现的认识和诊断。

21 Trisomy : Observation on Extra 21 Chromosome Origin

21三体：额外21号染色体来源观察

Observation of Karyotype in a Female with X - Trisomy

X三体性患者的染色体观察

METHODS : Trisomy 16 mouse breeding ;

方法：Trisomy16鼠培育；

Observation on the Rate of Satellite Association in Young Couples with Trisomy 21 Offsprings

21-三体患儿的年轻双亲染色体随体联合率的研究

Clinical and cytogenetic studies of hematological malignancies with isolated trisomy 11

11例伴有单纯11三体恶性髓系血液病患者的临床和细胞遗传学分析

Advances in study on relationship between maternal deficiency of folic acid and fetal trisomy 21 syndrome

母体叶酸缺乏与胎儿21-三体综合征关系的研究

Dermatoglyphics Analysis of 107 Cases of 21 & Trisomy

107例先天愚型皮纹分析

Hematological Characteristics and Prognosis of Myelodysplastic Syndrome with Sole Trisomy 11

单纯11三体骨髓增生异常综合征的血液学特征与预后

Prenatal ultrasound study of trisomy 13 and 18

13及18三体综合征胎儿的产前超声筛查

An experimental study on the developmental malformations of the trisomy 18 NMRI mice

18号染色体三体NMRI小鼠发育畸形的实验研究