ライフサイエンスコーパス: chromosomal anomaly

1 syndrome (DS), is the most common congenital chromosomal anomaly.

2 exhibit a number of numerical and structural chromosomal anomalies.

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

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

5 bute to a significant fraction of recognized chromosomal anomalies.

6 h, were used to identify pregnancies without chromosomal anomalies.

7 e, presence of noncardiac abnormalities, and chromosomal anomalies.

8 less than 2.0 mm were at the lowest risk of chromosomal anomalies.

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

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

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

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

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

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

15 ironment and clone adaptability with complex chromosomal anomalies and somatic mutations in TP53, NSD

16 with a wide variety of genetic syndromes and chromosomal anomalies, and they are among the principal

17 g boys with hypospadias, occurred outside of chromosomal anomalies, and were validated in the NBDPN.

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

19 A variety of other chromosomal anomalies are associated with musculoskeleta

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

21 40% (95% CI, 0.77%-2.04%) when restricted to chromosomal anomalies beyond the commonly screened aneup

22 urgery within the first week of life, lethal chromosomal anomalies, death within 48 hours of admissio

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

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

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

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

27 t studies showed a possible association with chromosomal anomalies for levels less than 3.5 mm, but e

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

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

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

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

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

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

34 slucency less than 2.0 mm; the prevalence of chromosomal anomalies in this group was 0.5%.

35 ed DNA samples from 1566 individuals without chromosomal anomalies, including 454 BD probands with at

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

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

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

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

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

41 These chromosomal anomalies represent one of the most common c

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

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

44 An increased risk of chromosomal anomalies was associated with increasing nuc

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

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

47 Several chromosomal anomalies were detected in one of these tumo

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

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

50 Chromosomal anomalies were identified through all Ontari

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