遗传性疾病、先天性畸形、变形和染色体异常；
The insured suffers from inherited disease, congenital abnormality, deformation or chromosome abnormality.
NT增厚除了与染色体病密切相关外，还与先天性心脏病、胎儿畸形、贫血、感染等因素相关。
NT thickening is related to chromosomal syndromes closely, still to congenital heart disease, fetal abnormalities, anemia, infection factors.
波威利将某些由染色体失常造成的畸形胚胎与肿瘤相提并论，而于1914年提出假说：多出或失去某些特定染色体，将引发癌症。
Boveri likened some of the resulting malformed embryos to tumors and, in 1914, predicted that gains or losses of specific chromosomes would initiate cancer.
该研究成果非常重要，因为不正确的染色体分配可能会导致畸形和像癌症一样的疾病发生。
This finding is highly significant, since incorrect distribution of the chromosomes can lead to abnormalities and diseases such as cancer.
本文对糖尿病孕妇胎儿死产、流产及畸形率高的原因、染色体稳定性以及药物致畸等方面进行了讨论。
The increased SCE frequency in diabetics may account for higher incidence of fetal stillbirth, abortion and malformations in diabetic pregnancies.
采用乳牛外周血液淋巴细胞作短期培养，以空气干燥法制备染色体。对临床诊断为输卵管阻塞牛1例和生殖器官畸形牛5例进行细胞遗传学分析。
Comparetive chromosome studies wore carried out by means of short culture of lymphocytes from peripheral blood of 1 cow with simple salpingo obstruction and 5 cows with reproduction system problems.
腹裂、白内障及肾盂输尿管连接处梗阻与染色体或全前脑畸形无关。
Gastrochisis, cataracts, and ureteropelvic junction obstruction are not associated with chromosomal anomalies or holoprosencephaly.
孕妇本人或丈夫染色体携带者异常染色体检出率为33.33%（3/9）；胎儿畸形的异常染色体检出率为15.63%（5/32）。
The abnormal rate of pregnant woman or husband chromosome sickness that carried unusual chromosome and malformed fetuses were 33.33%(3/9) and 15.63% (5/32), respectively.
所查杯状耳均无耳聋病史及其它部位畸形。结论：杯状耳的形成是由父母双方中一方杯状耳基因决定的，家系分析显示为常染色体显性遗传。
Conclusion:The family investigation suggested that the formation of cup ear was determined by the cup ear gene of an affected parent and it was an autosomal dominant inheritance.
与染色体异常有关的畸形主要包括多发畸形、心脏畸形、胎儿水肿、消化道畸形等。
Abnormal chromosome-related malformations mainly included multi-malformation, heart malformation, fetal edema and digestive malformation.
CPAP的某些突变诱导神经发育紊乱疾病“常染色体隐性小脑畸形(MCPH)”导致人类大脑生长的严重缩小。
Mutation of CPAP induces a neuro-developmental disorder named MCPH (autosomal recessive primary microcephaly) that causes a great reduction in brain growth in human.
CPAP的某些突变诱导神经发育紊乱疾病“常染色体隐性小脑畸形(MCPH)”导致人类大脑生长的严重缩小。
Mutation of CPAP induces a neuro-developmental disorder named MCPH (autosomal recessive primary microcephaly) that causes a great reduction in brain growth in human.
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