ライフサイエンスコーパス: chromosomal anomaly

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1 birth defect that is often caused by de novo chromosomal anomalies.

2 omal anomalies similar to that found for non-chromosomal anomalies.

3 bute to a significant fraction of recognized chromosomal anomalies.

4 ome wide as well as numerical and structural chromosomal anomalies.

5 ular system anomalies, 79.1% (76.7-81.3) for chromosomal anomalies, 93.2% (91.6-94.5) for urinary sys

6 Here, we studied 245 cases of chromosomal anomalies and 2412 controls who lived near 2

7 s not known, although teratogens, non-random chromosomal anomalies and familial forms with autosomal

8 telomeres, increased numbers of spontaneous chromosomal anomalies and higher frequencies of transfor

9 d FBXL2 triggered G2/M-phase arrest, induced chromosomal anomalies and increased apoptosis of transfo

10 ects revealed that previous cardiac surgery, chromosomal anomaly, and delayed sternal closure were in

11 A variety of other chromosomal anomalies are associated with musculoskeleta

12 We also demonstrate that MMC-induced chromosomal anomalies are increased in SNM1B-depleted ce

13 g surgical repair at <7 days of life, lethal chromosomal anomaly, death within 48 hours, inability to

14 We detected clonal mosaicism for large chromosomal anomalies (duplications, deletions and unipa

15 ng method for neural tube defects and common chromosomal anomalies during prenatal care.

16 ic testing has led to increased detection of chromosomal anomalies early in pregnancy.

17 abolic acidosis and noncardiac structural or chromosomal anomalies had higher mortality.

18 role of diabetes mellitus in the etiology of chromosomal anomalies has been infrequently studied.

19 ve PCR analysis to identify, confirm and map chromosomal anomalies in a cohort of 26 CDH+ patients.

20 blocks are reliable methods for detection of chromosomal anomalies in archival tissue of prostate can

21 ts, oral clefts, abdominal wall defects, and chromosomal anomalies in Hawaii by using actively ascert

22 ioeconomic status, we noted a higher risk of chromosomal anomalies in people who lived close to sites

23 mary congenital glaucoma (PCG) patients with chromosomal anomalies involving 6p25.

24 n protein) and may also provide evidence for chromosomal anomalies involving the NPM gene other than

25 N study showed a 33% increase in risk of non-chromosomal anomalies near hazardous waste landfill site

26 at 10 years and was shorter in patients with chromosomal anomalies, older age, a greater number of co

27 ity owing to a wide range of gene mutations, chromosomal anomalies or environmental insults.

28 These chromosomal anomalies represent one of the most common c

29 Our results suggest an increase in risk of chromosomal anomalies similar to that found for non-chro

30 N+IL-15 was positively linked to presence of chromosomal anomalies (trisomy-12 or ataxia telangiectas

31 cted major, non-chromosomal birth defects or chromosomal anomalies was compared to a reference cohort

32 Conversely, intratumor heterogeneity of chromosomal anomalies was identified in 5 cases by FISH

33 Several chromosomal anomalies were detected in one of these tumo

34 Numeric chromosomal anomalies were found in 67, 68, and 96% of f

35 In prostatic carcinoma, numeric chromosomal anomalies were found in 75% of cases by both

36 Comet analysis showed that these extensive chromosomal anomalies were not due to increased inductio

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