查询词典 trisomy

Cases of trisomy 21 were identified from the cytogenetics laboratory logbook .

Down综合征（21三体综合症）的鉴别参照细胞遗传学手册。

Methods To analyze retrospectively the ultrasonography of 8 cases which had been karyotyped to be trisomy 18 by fetal blood sampling or amniocentesis.

对脐血或羊水染色体核型分析确诊为18三体综合征的8例胎儿超声声像图进行回顾性分析。

It is interesting that the gene coding for cerebral amyloid is on chromosome 21--and persons with trisomy 21 living to age 40 invariably develop Alzheimer's disease.

有趣的是，淀粉样蛋白遗传密码位于21号染色体上，并且活到40岁的21三体症患者出现Alzheimer病不尽相同。

Besides, he also suffered from congenital hydrocephalus and hypogammaglobulinemia, which have not been described in trisomy lq syndrome.

除此之外，他还并发先天性水及及免疫球蛋白低下等两项以前在部分三染色体第一号症候群尚未被报告过的症状。

Synchronous firing trisomy has been used many calligraphy lovers, has a scientific nature, is entirely possible to allow the use of learning calligraphy are ways to practice calligraphy.

同步练三体已被众多的书法爱好者采用，有科学性的，完全可以让初学书法者运用的练字途径。

It was original report to find the developmental delay of the ENS, absence of submucosal plexus and the aganglionic segment of colon ending in trisomy 16 mice, an animal model for Down syndrome.

Down综合征的动物模型常染色体16三体胎鼠ENS发育迟缓，粘膜下神经丛发育障碍出现后肠末端无神经节区。

Chromosomal abnormalities were identified in two anencephalic fetuses. One was trisomy 21, another was mosaic of diploid and tetraploid.

1。组织病理学和超微病理发现，NTDs胎儿在脑和脊髓以及重要脏器如肝、肾等发育有异常，主要表现在发育滞后和某些成分的缺如。

The phenotype of partial trisomy 1 and partial monosomy X of the present case was much attenuated, including premature ovarian failure, mental retardation, class I obesity, mild dysmorphism, and delayed secondary sexual characteristics.

该患者主要存在卵巢早衰、智力障碍，I度肥胖，轻微畸形以及第二性征发育迟缓等，与单纯的部分1－三体综合症等相比表型大大弱化。

Refers to Down's syndrome (Down's syndrome, dementia-like伸舌) screening, that is, pumping blood or amniotic fluid do villus cells, and then do Karyotype analysis, such as the emergence of 21 - trisomy map, you can diagnose fetus for Down syndrome. 2, AFP Chinese name for the AFP, such as maternal and fetal amniotic fluid were increased AFP confirmed fetal neural tube defects, namely spina bifida, spinal Meningocele, no brains infants, microcephaly, hydrocephalus.

是指唐氏综合症的筛查，就是抽绒毛血或羊水做细胞培养，然后做染色体核型分析，如出现21-三体综合征图谱，即可诊断胎儿为唐氏综合征。2、AFP中文名称为甲胎蛋白，如母血及胎儿羊水AFP均增高，证实胎儿有神经管畸形，即脊柱裂、脊脑膜膨出、无脑儿、小头畸形、脑积水。

Using CCA, karyotype abnormalities were found in 18 (37.5%) of 48 cases, among which complex karyotypes were found in 4 (8.3%) cases, a deletion of chromosome 5/a deletion of the long arm of chromosome 5 (-5/5q-) in 5 (10.4%) cases,-7/7q- in 5 (10.4%) cases, trisomy 8 in 8 (16.6%) cases, 20q- in 2 (4.6%) cases, unconsistent translocations in 3 (6.2%) cases.

细胞遗传学分析检出染色体异常18例(37.5%)，其中复杂异常4例(8.3%)、5号染色体缺失或5号染色体长臂部分缺失5例(10.4%)、7号染色体缺失或7号染色体长臂部分缺失5例(10.4%)、8号染色体增加8例（16.6%）、20号染色体长臂部分缺失2例（4.6%）、不一致的易位3例（6.2%）。

As she looked at Warrington's manly face, and dark, melancholy eyes, she had settled in her mind that he must have been the victim of an unhappy attachment.

每逢看到沃林顿那刚毅的脸，那乌黑、忧郁的眼睛，她便会相信，他一定作过不幸的爱情的受害者。

Maybe they'll disappear into a pothole.

也许他们将在壶穴里消失