英语人>词典>汉英 : 两性畸形的 的英文翻译,例句
两性畸形的 的英文翻译、例句

两性畸形的

基本解释 (translations)
bisexed  ·  gynandromorphous

更多网络例句与两性畸形的相关的网络例句 [注:此内容来源于网络,仅供参考]

Objective This paper evaluates the importance of early diagnosis and systemic treatment of true hermaphroditism.

目的 探讨真两性畸形的早期正确诊断与合理治疗。

We herein report two cases of goats with sexual deformity.They had two systems of reproductive organs and the karyotype analysis showed mosaicism for their sex chromosomes,i.e.,60,XX / XY.The proportion of XX cell line was 42% and 54%,while XY cell line was 58% and 46%,respectively,in the two abnormal goats.

本文报道2例两性畸形的山羊,它们均具雌雄两套生殖器官,染色体组型分析显示它们均为性染色体嵌合体,核型为60,XX/XY,两头畸形山羊的XX细胞系的比例分别为42%和54%,XY细胞系的比例分别为58%和46%。

Fig 3 Male pseudohermaphrodite raised as a female,Preopera-tive and 7 days postoperatively

图3抚养为女性的男性假两性畸形,术前和术后7d

Methods The CT findings in 4 cases of female pseudohermaphroditism were analyzed retrospectively.

回顾性分析4例经手术及临床诊断为女性假两性畸形的CT表现。

Objective To evaluate the CT findings of female pseudohermaphroditism.

目的 评价女性假两性畸形的CT表现特点及其临床价值。

Objective To evaluate the CT findings of female pseudohermaphroditism. Methods The CT findings in 4 cases of female pseudohermaphroditism were analyzed retrospectively.

目的 评价女性假两性畸形的CT表现特点及其临床价值方法回顾性分析4例经手术及临床诊断女性假两性畸形的CT表现。

Objective To evaluate the diagnosis and treatment of female pseudohermaphroditism caused by 21-hydroxylase deficiency.

目的 探讨21-羟化酶缺乏(21-hydroxylase deficiency,21-OHD)致女性假两性畸形的临床诊断及治疗方法。

You've got male pseudohermaphroditism.

你患的是男性假两性畸形

DNAs from a group of sex chromosome abnormal patients〔46 XX male, 45 XO Turner's syndrome, 47 XXY klinelfter syndromes, 46 XX true hermaphrodite, 46 XY hermaphrodite, 47 XYY male, 48 XXXY male〕 was hybridized to ZFT using southern bloting method.

我们对一组性染色体异常的病人(46XX男性,46XX真两性畸形,46XY两性畸形,45XO Turner's综合症,47XXY Klinelfter综合症,47XYY男性,48XXXY男性)DNA,用ZFY探针进行了Southern印迹杂交。

The results showed that all of them could detect the presence of ZFY DNA sequences except a 46 XX"male"and a 46 XX hermaphrodite, our findings confirmed that Ferguson-Smith〔1966〕 forwarded the hypothesis that the X-Y intercharge model for XX maleness can be regarded as an abnormal exchange initaited in a region proximal to TDF and extending to the telomere,and,also strongly suggested that ZFY gene palyed an important role in sex determining of human.

结果除一例46XX两性畸形,一例46XX&男性&外,余均能检测到ZFY DNA序列(ZFY DNA序列存在于46XX真两性畸形和45XO Turner's综合症,在国内外尚未见报道)。证实了1966年,Ferguson-Smith提出的理论:在父源减数分裂期间,X-Y发生不等交换,导致Y染色体DNA插入性易位。XX男性是由于Y染色体上的TDF基因转移至X染色体上所致。

更多网络解释与两性畸形的相关的网络解释 [注:此内容来源于网络,仅供参考]

amphimixis:两性混合

两性反应的amphichroic | 两性混合amphimixis | 两性畸形hermaphrodism

Hermaphrodite:两性畸形人

hermaic 方形石柱的 | hermaphrodite 两性畸形人 | hermaphroditic 两性的

hermaphroditism:两性畸形

两性畸形(hermaphroditism)分为假两性畸形和真两性畸形. 假两性畸形是遗传性别、性腺性别和表型性别的不均一性,即性腺性别与遗传性别一致,而生殖导管和尿生殖窦的发育却具有异性的成分或兼有两性的特征. 以遗传性别和性腺性别为基础,

true hermaphroditism:真两性畸形

临床表现外生殖器曾受睾酮的影响,如阴蒂稍增大,会阴体部分融合. 因睾丸退化外生殖器不再发育. 处理同XY 单纯性腺发育不全,并行外阴整形. 3.真两性畸形(true hermaphroditism)此类患者染色体正常,但性腺同时具有睾丸和卵巢两种成分,为真两性.

Male with sex chromosome mosaicism:男性,伴有性染色体(同源)嵌合体的

男性假两性畸形 Male pseudohermaphroditism not elsewhere cla... | 男性,伴有性染色体(同源)嵌合体的 Male with sex chromosome mosaicism | 男性,伴有结构异常的性染色体的 Male with structurally abnormal sex c...

pseudohermaphrodite:假半阴阳的人; 假两性畸形的人 (名)

pseudograph 伪作; 伪书 (名) | pseudohermaphrodite 假半阴阳的人; 假两性畸形的人 (名) | pseudonym 假名; 雅号; 笔名 (名)

pseudohermaphroditism:假两性畸形

什么是肾上腺性征异常症?肾上腺性征异常症是由于过多的肾上腺雄性激素所致之性征异常,致女性男化(virilism)男性早熟. 而在成年男性难以确定其临床情况. 这一症征,在女性的表现是假两性畸形(pseudohermaphroditism),其肾上腺皮层增厚. 在1866年creechio已有记载,但

male pseudohermaphroditism:男性假两性畸形

(2)男性假两性畸形 男性假两性畸形(male pseudohermaphroditism)的患儿,细胞染色体核型为男性46,XY,性腺为睾丸或缺无,其原因比较复杂,见表31-17. ①性腺发育不全 性染色体为XY的完全性或部分性的性腺发育不全,有H-Y抗原阳性的完全性或部分性性腺发育不全和睾丸分化不良.

female pseudohermaphroditism:女假两性畸形

女假两性畸形(female pseudohermaphroditism)的共同特点为:性染色体XX,性染色质阳性,具有卵巢组织,畸形主要表现为外阴部程度不等的男性化. 先天性肾上腺皮质增生是女假两性体的主要原因,而且外生殖器非男非女者约半数都由此种病变造成.

bisexed:两性畸形的,半阴阳的,雌雄同体的

bisette | 刺绣辫带, 白亚麻枕套花边, 廉价花边 | bisexed | 两性畸形的,半阴阳的,雌雄同体的 | bisexual reproduction | 两性生殖