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chromosome 12相关的网络例句

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与 chromosome 12 相关的网络例句 [注:此内容来源于网络,仅供参考]

For suspected cases, in early pregnancy (8-12 weeks), chorionicvilluscell karyotype analysis was done in those with spontaneous natural abortion; in the midtrimester (13-24 weeks) and the late pregnancy (over 25 weeks), the abortus or newborn blood was collected for chromosome analysis.

对有胎儿异常可能的病例,孕早期(8~12周)自然流产者行绒毛细胞核型分析,孕中期(13~24周)及晚期(25周以上)取流产儿和新生儿血进行染色体分析。

Segregation distortions were found on chromosome 1, 2, 3, 6, 10, 11 and 12 respectively. There were some distorted markers clustered in special regions on chromosome 3, 6 and 11, and they all deviated toward indica homozygote.

不平衡分离发生在第1、2、3、6、10、11、12条染色体上,其中第3、6、11条染色体上发生不平衡分离的分子标记有「群集」的现象,且三者都倾向於秈稻同质结合型。

In the 34 observed chromosome aberration cells, the micronucleus number had 5 types of 8, 9, 10, 11 and 12, among them, the chromosome aberration cells with 10 and 11 micronuclei were the most.

在所观察的34个染色体畸变细胞中微核数有5种类型(8、9、10、11、12),其中以微核数10和11的染色体畸变细胞为主。

That could be the results of unequal misdivision of wheat_rye 1BL/1RS translocation chromosome and Thinopyrum chromosome during meiosis.

在遗 42 12×遗 40 95的F2 代中检测到一个具有中间偃麦草染色体小片段易位到小麦染色体端粒部分的小麦_中间偃麦草易位植株。

Results Mosaicism analysis was performed on 14 normal fertilized embryos, which had more than two cells. Nine embryos had sex chromosome mosaicism. XO in male and female embryos cells were 12%and 14%respectively.

结果 有两个细胞以上的14个正常受精胚胎中9个胚胎有不同程度的性染色体嵌合,其中男性胚胎41个细胞中XO有5个,占12%;女性胚胎28个细胞中XO有4个,占14%。

Nine embryos had sex chromosome mosaicism. XO in male and female embryos cells were 12% and 14% respectively. Conclusion Identification of sex by FISH analysis of a single cleavage cell is accurate, and sex chromosome mosaicism will not affect preimplantation gender diagnosis.

结果 有两个细胞以上的14个正常受精胚胎中9个胚胎有不同程度的性染色体嵌合,其中男性胚胎41个细胞中XO有5个,占12%;女性胚胎28个细胞中XO有4个,占14%。

Experiment result shows that 1.there are totally 26 chromosomes;2.chromosome 1,2,5,7,8,10,12 have central centromeres;chromosome3,4,6,9,11,13 have vise central centromeres;sex chromosome cannot be detected.

实验结果显示,其染色体共有2n=26条,其中其中1,2,5,7,8,10,12为中部着丝粒;3,4,6,9,11,13为亚中部着丝粒,性染色体无法分辨。

Results: Twenty eight out of 57 patients had clonal chromosome aberrations. Among the 28 aberrational chromosome,+8 presented in 8 cases, t (8; 21) translocation in 4 cases, 20q-in 2 cases, i (20q-) which was an rare recurrent chromosome abnormality in 1 case, and complex karyotype in 7 cases, but 5q-was not found in all the patients.

结果:MDS患者中异常核型率为49.12%(28/57)。28例异常核型患者中伴有+8异常8例,t(8; 21)易位4例,20q-2例,少见的重现性异常i(20q-)1例,复杂核型7例,未见5q-核型。

It was found that one of the fragments was similar to the Peroxidase gene located on the rice chromosome 1 completely, another fragment was partially similar to the protein Phosphorylase gene located on the rice chromosome 12 with 99.99% homology.

同源性均在99%以上。其中一个与位于水稻第一号染色体的过氧化物酶基因的部分片段有100%相似性。另一个与位于第十二号染色体上的蛋白磷酸化酶基因有99.99%的同源性。

All lines showed a chromosome number of 2n = 42, five of them carried botha pair of wheat-rye (Triticum aestivum-Secale cereal ) 1BL/1RS translocation chromosomes and a pair ofAgropyron intermedium chromosomes, three carried a pair of Ai chromosomes only, three otherscarried a pair of 1BL/1RS chromosomes only, and one carried neither 1BL/1BS nor Ai chromosome.

结果表明,12份材料染色体数均为42,其中5份材料均具有一对小麦-黑麦(Triticum aestivum-Secalecereal)1BL/1RS易位染色体和一对中间偃麦草染色体、3份材料只具有一对中间偃麦草染色体、3份材料只具一对1BL/1RS染色体、1份材料无1BL/1RS和中间偃麦草染色体。

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