英语释义

• chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell

片语

partial trisomy部分三体型

trisomy 8三体

primary trisomy三体染色体

trisomy-三染色体细胞；三染色体性

trisomy detail三体性

Trisomy 2121三体

trisomy monosomy三体型

-trisomy三染色体细胞；三染色体性

e trisomy三体综合征

英汉例句

• synchronous firing trisomy has been used many calligraphy lovers, yes there is scientific in nature, are totally beginner can practice calligraphy calligraphy are used via.

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

• if this is a patient with trisomy 21, it become more complicated.

  如果这病人是21三体， 可能就复杂些。

• materials and methods:cerebral ct findings in 23 cases with 21 trisomy syndrome, proved by cytogenetics, were retrospectively analyzed.

  材料与方法：回顾性分析23例经细胞遗传学检查证实的21三体综合征的脑部ct表现。

• the detection rate of the chromosomal abnormality of the abnormal fetus detected by ultrasound (33.33%) was higer than the trisomy 21 high risk group(4.54%) and abnormal delivery group(9.09%)(p0.05).

  其中超声示胎儿异常组染色体异常检出率（33.33%）明显高于21-三体高风险组（4.54%）、不良孕产史组的检出率（9.09%）（p0.05）。

• object:to evaluate the prognostic impact of trisomy 8 on cytobiological and clinical features in acute myelomonocytic and monocytic leukemia (m4, m5).

  目的探讨8号染色体三体（8三体）对急性粒单、单核细胞白血病（m4、m5）细胞生物学及临床特征的影响。

• objective:to evaluate sonographic characteristics on prenatal ultrasound study of trisomy 13 and 18…

  目的：对13及18三体综合征胎儿的超声表现特征和产前超声筛查价值的评价。

• low levels of all three serum analytes identifies 60-75% of all cases of fetal trisomy 18.

  当这三个值均低时则可考虑18-三体综合征，阳性率为60-75％。

• objective:a few trisomy 21 cells in normal chromosome karyotype was been observed for study of the correlation of clinical phenotype and development damage in sick children of down「s syndrome.

  目的观察正常细胞核型中含有极少量21-三体细胞的患儿临床表型及发育损害的相关关系。

• conclusion trisomy 16 mice occur with congenital megacolon, and trisomy 16 mice may be also regard as an animal model for hirschsprung」s disease.

  结论唐氏综合征动物模型16三体鼠伴有先天性巨结肠，这种动物模型可用于研究先天性巨结肠病。

• results: the trisomy with cleft palate mouse foetuses had significantly developmental hypoplasia in the primary palatal shelves.

  结果：该模型虽无原发腭裂却伴有原发腭的发育不足；

• results nine cases of trisomy 18 and 2 cases of other abnormal karyotype were found among the 128 pregnant women (8.59%, 11/128).

  结果128例胎儿核型中，9例为18三体综合征，2例为其它染色体异常，染色体异常发现率为8·59%（11/128）。

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

  三体综合癥在医学研究上备受关注，但其确切机制仍未明确。

• 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。

• zhao x. , sun h. -x. , hu y. -l. establishment of a human embryonic stem cell line with trisomy 16.

  招霞，孙海翔，胡娅莉染色体16三体人胚胎干细胞系的建立★。

• objective to investigate the frequency of trisomy 8 in acute lymphoblastic leukemia(all).

  目的探讨急性淋巴细胞白血病（all）中8号染色体三体（8三体）的发生率。

• one of the ideas that i am working on is that if a patient has trisomy 7 only we can give them an epidermal growth factor receptor inhibitor for six months and see if we can eradicate those clones.

  在这方面我正在研究的一种思路就是，如果一个患者只有7三体，我们可以用表皮生长因子受体阻滞剂治疗6个月，观察是否能根除这种克隆。

• this confirmed the presence of tetrasomy 8 and trisomy 8 and also revealed a low percentage of a pentasomy 8 clone.

  这不但证实了三体8和四体8克隆的存在，还发现存在一个较小的五体8克隆。

• objective:to determine the rate of prenatal detection of ultrasonography abnormalities in fetuses with trisomy 18 and evaluate its predictive value.

  目的：探讨孕期18-三体胎儿超声异常的产前检出率及临床价值。

• objective: to improve the understanding and diagnostic ability of the brain changes in 21 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。

• a short femur is associated with trisomy 21 rather than trisomy 13 and holoprosencephaly.

  股骨短与21-三体而不是13-三体或全前脑畸形有关。

• you live in italics, li you-ling body, the expensive solid body. trisomy trained with each other.

  楷体贵活，隶体贵灵，行体贵稳。三体同练就能互补。

• objective to explore the value of interphase fluorescence in situ hybridization(i-fish) on the detection of trisomy 8 in chronic myeloid leukemia(cml) and the progression of cml.

  目的探讨间期荧光原位杂交（i-fish）技术检测慢性髓系白血病（cml）8号染色体三体（8三体）异常的价值及其对cml演进监测的意义。