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   genetic counseling 的翻译结果: 查询用时:0.185秒
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genetic counseling
相关语句
  遗传咨询
     RARE CHROMOSOME TRANSLOCATION t(6;9)(q23:p24) AND GENETIC COUNSELING (REPORT OF 1 CASE)
     1例罕见的染色体易位t(6;9)(q23;p24)及其遗传咨询
短句来源
     Conclusion The EcoRⅠ-BlnⅠ/p13E-11 fragment size is negatively correlated with FSHD 1A clinical severity. It is a major factor in determining the FSHD 1A clinical severity and has an impact on clinical prognosis and genetic counseling of the disease.
     结论EcoRⅠ+BlnⅠ/p13E-11DNA片段大小与FSHD1A的临床表型之间具有负相关性,它在判断FSHD1A病情预后以及遗传咨询方面具有重要参考价值。
短句来源
     Her phenotype is normal and karyotype of chromosome shows 46 ,ⅩⅩ, t(6;9) (6pter→6q23::9p24→9pter;9qter→9p24::6q23→6qter). It is the first report in literature. We have taken the genetic counseling to the patient.
     其表型正常,该染色体核型为46,XX,t(6;9)(6pter→6q23::9p24→9pter;9qter→9p24::6q23→6qter),国内外尚未见报道,并对其进行了遗传咨询
短句来源
     Objective:To analyze chromosome karyotype of the couples in early recurrent spontaneous abortion and offer the genetic counseling for the next pregnancy.
     目的:对反复早期自然流产的夫妇进行染色体分析,探讨反复早期自然流产与染色体异常的关系,为再次妊娠提供遗传咨询
短句来源
     Analysis of 400 Attendant Cases in Genetic Counseling Clinic
     遗传咨询门诊400例分析
短句来源
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  遗传咨询者
     Cytogenetic Analysis on 400 Genetic Counseling Patients
     400例遗传咨询者细胞遗传学分析
短句来源
     Chromosome analysis of peripheral blood from 508 individual of genetic counseling
     508例遗传咨询者外周血染色体分析
短句来源
     A cytogenetic study of 630 patients for genetic counseling
     630例遗传咨询者的细胞遗传学研究
短句来源
     Results We analysis the 211 people genetic counseling peripheral lymphocytes chromoseme. Chomosomal abnormal kanruyotypes were found 19 cases(9.00%).
     结果分析延安市遗传咨询者211例的外周血染色体,发现异常核型19例,占9.00%。
短句来源
     The study of cytogenetics in the 1218 cases of genetic counseling
     贵州省1218例遗传咨询者的细胞遗传学研究和分析
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  “genetic counseling”译为未确定词的双语例句
     47,XXX Syndrome and Its Genetic Counseling Methods
     47,XXX综合征的研究进展
短句来源
     Genetic counseling of 22 patients of balanced translocation carrier.
     22例染色体平衡易位携带者优生遗传咨询
短句来源
     Chromosome Analysis of 1133 Cases in Genetic Counseling Clinic
     1133例遗传门诊病例的细胞遗传学分析
短句来源
     Robertson translocation t(15;21) in 3 generations 1 family as well as birth health genetic counseling
     一家三代Robertson易位t(15;21)及其优生遗传咨询的探讨
短句来源
     The FMR-1 gene mutation and Xq27.3 fragile site among 233 non-specific mentally retarded children were investigated in our genetic counseling department and two special educational schools by PCR, Southern Blot hybridization and cytogenetic methods.
     采用PCR、Southern Blot印迹杂交及细胞遗传学方法,对233名原发性智力低下患儿进行了FMR-1基因的突变分析和Xq27.3脆性位点检查。
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  genetic counseling
Molecular screening of probands" relatives will contribute to identification and medical genetic counseling of heterozygous carriers, which is essential for CF prevention.
      
The data on the genetics and epidemiology of mitochondrial diseases are not only important for differential diagnosis and genetic counseling.
      
The results of this study can be used in medical genetic counseling for identifying subjects at high risk for schizophrenia.
      
Protocols were developed for direct or indirect DNA diagnostics of the diseases under study to improve medical genetic counseling and prevention of new disease cases in affected families.
      
Cornerstones of clinical management comprise genetic counseling, life-style management, and cardiovascular surveillance, which includes regular aortic imaging and endocarditis prophylaxis.
      
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Four cases from two families suffering from both bony abnormalities of the upper extremity and cardiac defects (Holt-Oram syndrome) are reported. The embryologic and hereditary bases for the association of such defects are discussed briefly.The Holt-Oram syndrome is known as an autosomal dominant disease. A search for associated skeletal abnormalities is justified in order to: 1. help make a coriect diagnosis, 2 find out other patients in the same family, 3. offer appropriate genetic counseling for patients...

Four cases from two families suffering from both bony abnormalities of the upper extremity and cardiac defects (Holt-Oram syndrome) are reported. The embryologic and hereditary bases for the association of such defects are discussed briefly.The Holt-Oram syndrome is known as an autosomal dominant disease. A search for associated skeletal abnormalities is justified in order to: 1. help make a coriect diagnosis, 2 find out other patients in the same family, 3. offer appropriate genetic counseling for patients and their parents, and 4. alert the physicians to the possibility of peripheral vascular hypoplasia, variable arrhythmias and their attendant complications.

本文报告了来自两个家族的4例上肢心血管综合征病例,对其胚胎学和遗传学因素作了扼要的讨论。本综合征是一种常染色体显性遗传性疾病,注意合并的上肢畸形有助于确诊和在同一家族中找出其他患者。在诊疗中应注意可能存在的各种心律失常和外周血管畸形。对患者和家属应提出适当的遗传方面的忠告。

This study reports a new method of fetal blood sampling by placental aspiration and purification to get a pure fetal red blood cell sample for the use of prenatal diagnosis in certain inherital diseases.This procedure had been performed in 78 pregnant women scheduled to have termination of midtrimester pregnancy and 2 cases required genetic counseling.These samples thus obtained contained both maternal and fetal red blood cells and the account of the fetal RBC sampled from O to 99%.There were 67 samples...

This study reports a new method of fetal blood sampling by placental aspiration and purification to get a pure fetal red blood cell sample for the use of prenatal diagnosis in certain inherital diseases.This procedure had been performed in 78 pregnant women scheduled to have termination of midtrimester pregnancy and 2 cases required genetic counseling.These samples thus obtained contained both maternal and fetal red blood cells and the account of the fetal RBC sampled from O to 99%.There were 67 samples containing fetal RBC more than 3%,all but 1 case,because account of sample was too little,and was treated by the method of adult RBC selective hemolysis to get pure or nearly pure fetal RBC samples.The successful rate of the procedure was 83.75%,and no untoward reaction was observed.The G6PD activity measure and.the microhemog-lobulin electrophoresis test of the purifical fetal RBC samples evidence that the purified fetal RBC can be used for prenatal diagnosis of inherited diseases such as hemoglobinopathies and erythrocyte enzyme defects.

80例妊娠15~28周中期妊娠引产和遗传咨询的孕妇,经胎盘抽吸胎血取样所获得的血样中,胎儿红细胞比例为0~99%。胎儿红细胞3%以上,能经成人红细胞选择性溶血法分离得到纯或较纯的胎儿红细胞标本的血样67例。胎血取样成功率为83.75%。纯化的胎儿红细胞G6PD活性测定和微量血红蛋白电泳检查表明:纯化的胎儿红细胞可用于血红蛋白病和红细胞酶缺陷等遗传性疾病的产前诊断。

Amenorrhea is one of the conimonest diseases in gynecology. Twelve cases of primary amenorrliea were encountered at our genetic counseling clinic from April 1982 to Februaryl985. Four cases of this series have a normal female karyotype, 46, XX; among them, three are of the congenital anomaly with no vagina and uterus. Six cases are diagnosed as gonadal (ovarian) dysgenesis (Turner's syndrome), and their kar~ yotyping are 45—XO; 46—X, i (Xq) ; 45— XO/46—X, i (Xq) /47—X, i (XqXq) and 45—XO/46, XXp respectively....

Amenorrhea is one of the conimonest diseases in gynecology. Twelve cases of primary amenorrliea were encountered at our genetic counseling clinic from April 1982 to Februaryl985. Four cases of this series have a normal female karyotype, 46, XX; among them, three are of the congenital anomaly with no vagina and uterus. Six cases are diagnosed as gonadal (ovarian) dysgenesis (Turner's syndrome), and their kar~ yotyping are 45—XO; 46—X, i (Xq) ; 45— XO/46—X, i (Xq) /47—X, i (XqXq) and 45—XO/46, XXp respectively. Besides, there are two remaining cases showing 46, XY karyotype, one being pure XY gonada(?) dysgenesis; the other being a phenotypic girl with syndrome of testiular feminization, which is of a male pseudohermaphonoditism nature

闭经是妇科常见病之一。从1982年4月~85年2月,我们在遗传咨询门诊遇到12例原发性闭经患者,其中4例染色体核型正常,均为46,XX;内三例诊断为先天性无阴道无子宫;6例先天性卵巢发育不全症(特纳氏综合征),核性分别为45,XO;46,X,i(Xq);45,XO/46,X,i(Xq)/47,X,i(XqXq)和45,XO/46,XXp~-。一例真性XY性腺发育不全症,染色体核型为46,XY。另一例睾丸女性化,染色体核型亦为46,XY,属男性假两性畸形。

 
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