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号染色体

网络web; Chromosome; touchscreen

号染色体

号染色体

号染色体

web

维基百科:最多语言版本的待撰条目 -... ... 无虹膜 keyboard 17号染色体 (人类) web 畸形足 device database ...

Chromosome

别让宝宝缺陷与生俱来|怀孕 ... 缺陷凶手：21号染色体（ Chromosome ）数目异常（如染色体（ Chromosome ） ...

touchscreen

维基百科:最多语言版本的待撰... ... 13号染色体 (人类) jQuery 16号染色体 (人类) touchscreen 脂尾袋鼬 en:Fat-tailed dunnart ...

jQuery

维基百科:最多语言版本的待撰... ... 灰葡萄孢菌 en:Botrytis cinerea 13号染色体 (人类) jQuery 16号染色体 (人类) touchscreen ...

2

Chris Hammond , at King 's College , London, found one section of DNA on chromosome 15 was more common in people with myopia .

伦敦大学国王学院的克里斯•哈蒙德发现，15 号染色体上的一个 DNA 片段更常见于近视患者。

3

Conclusion In GIST there was heteroploid of chromosome 8 with more polyploidy than monoploid correlated with recurrence and metastasis.

结论 GIST 中存在 8 号染色体的数目异常，多倍体多于单倍体，并且与 GIST 复发转移有关；

5

The altered portion of chromosome 16 has structural characteristics that make it more prone to errors , Scherer noted .

Schere 指出，16 号染色体被改变的部分拥有更容易出错的结构特征。

7

The sequence of chromosome 21 was a turning point for the understanding of Down syndrome .

序列的 21 号染色体是一个转折点的理解唐氏综合征。

8

En route to constructing such a physical map of human chromosome 7, we have generated 1814 chromosome 7-specific STSs.

途中构建这种对人类 7 号染色体物理图谱，我们产生了 1814 年 7 号染色体的特定点图。

9

As a tumor -suppressor gene , phosphatase and tensin homology deleted on chromosome 10(PTEN) regulates negatively the growth of tumor cells .

第10 号染色体同源丢失性磷酸酶 -张力蛋白基因（PTEN ）作为肿瘤抑制基因，可以负性调节肿瘤细胞的生长。

10

11

In 1995 , the first news of a genetic basis for bed-wetting made headlines, after Danish researchers reported a link to Chromosome 13 .

1995年，在丹麦研究人员发表关于 13 号染色体的文章之后，第一则关于 “尿床的遗传因素 ”的消息曾引起轰动。

12

Angelman syndrome is associated with a mutation on the mother 's chromosome 15 .

安格尔曼综合征则是由来自于母亲的 15 号染色体突变所导致的。

13

It is concluded that the aberration of chromosome 5 is common in myeloid malignancies, and presents unbalanced translocation.

结论：髓系恶性血液病复杂核型异常中 5 号染色体异常多见，多为不平衡易位；

15

Of those genes on chromosome 21 that McLysaght has identified as being dosage-sensitive , many have already been linked to Down's syndrome .

在 21 号染色体的基因上边，McLysaght 已经鉴定出将要敏感的基因，当中许多都与唐氏综合症有关。

16

Only nine non-polymorphic constitutional pericentric inversions of chromosome 9 have been described .

只有 9 个非多态性的组成型 9 号染色体臂间倒位被描述。

17

Often , the error resulted in an extra copy of chromosome 21 , which causes Down 's syndrome .

通常情况下，错误导致 21 号染色体的多余复制，引发唐氏综合症。

18

According to a study published in the journal Nature , the genes in question are a group of 28 that form part of chromosome 16 .

根据一项发表在《自然》杂志的研究，这类 “瘦身 ”基因由人类第16 号染色体上的 28 个基因组成。

19

a congenital disorder caused by having an extra 21st chromosome ; results in a flat face and short stature and mental retardation .

有多一个号染色体的先天病症；病人有扁平脸和矮短体型，并且智力不足。

20

This revealed that CYP2E1 on chromosome 10 appears to dictate whether a person can hold their drink better than others .

这剖明，10 号染色体上的 CYP2E1 基因似乎可以抉择一小我能否在喝酒时比别人默示得更好。

21

These proteins are encoded by genes that are grouped on a part of chromosome 6 called the major histocompatibility complex , or MHC.

这些蛋白是由位于 6 号染色体上的一段称为主要组织相溶性复合体基因，MHC 编码的。

22

Prader-Willi syndrome is caused by a mutation in a father 's genes that deletes a chunk of DNA on chromosome 15.

普拉德 -威利综合征是由一个来自父方的染色体突变所引起，其 15 号染色体的 DNA 发生了大片段丢失。

23

Prader-Willi emerges from an opposite breakdown , in which the father 's DNA in the same segment of chromosome 15 is deleted.

普瑞德 -威利综合征则从出现完全相反的故障开始，也就是父方 15 号染色体 DNA 相同的片段丢失。

24

The investigations involved association analysis in the 51 families studied originally that showed linkage to chromosome 17 .

最初的研究发芽拜访涉及 51 个家庭的联系关系性剖析，数据剖明 17 号染色体与白癜风有关。

26

And the long arm of chromosome 13 was painted by human chromosome 20 library.

20 号探针杂交到恒河猴的 13 号染色体长臂上。

27

Objective: To investigate the clinical manifestation and the genetic effects for pericentric inversions of chromosome 9 in human.

目的探讨 9 号染色体臂间倒位的临床及遗传效应。

28

The disease gene is exactly located on the chromosome 5 and chromosome 12 through parameter and non-parameter linkage analysis .

综合运用参数和非参数连锁分析，将致病基因定位到 5 号染色体和 12 号染色体上。

29

Caroline Klaver, at Erasmus Medical Centre in Rotterdam, found another strand, also on chromosome 15, linked to short sight .

鹿特丹伊拉兹马斯医疗中心的卡洛琳克拉夫也在 15 号染色体上发现了另一串与近视有关的基因。

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