Cram D - Search Results

1

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y. Mao J, et al. Among authors: cram d. Clin Chim Acta. 2014 Jun 10;433:190-3. doi: 10.1016/j.cca.2014.03.011. Epub 2014 Mar 22. Clin Chim Acta. 2014. PMID: 24667696

2

Maternal X chromosome copy number variations are associated with discordant fetal sex chromosome aneuploidies detected by noninvasive prenatal testing.

Wang S, Huang S, Ma L, Liang L, Zhang J, Zhang J, Cram DS. Wang S, et al. Clin Chim Acta. 2015 Apr 15;444:113-6. doi: 10.1016/j.cca.2015.02.014. Epub 2015 Feb 14. Clin Chim Acta. 2015. PMID: 25689220

3

A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.

Wang T, Mao J, Liu MJ, Choy KW, Li HB, Cram DS, Li H, Chen Y. Wang T, et al. Clin Chim Acta. 2014 Mar 20;430:129-33. doi: 10.1016/j.cca.2014.01.002. Epub 2014 Jan 9. Clin Chim Acta. 2014. PMID: 24412318

4

Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART).

Lv W, Wei X, Guo R, Liu Q, Zheng Y, Chang J, Bai T, Li H, Zhang J, Song Z, Cram DS, Liang D, Wu L. Lv W, et al. Among authors: cram ds. Clin Chem. 2015 Jan;61(1):172-81. doi: 10.1373/clinchem.2014.229328. Epub 2014 Nov 6. Clin Chem. 2015. PMID: 25376582

5

Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.

Chen Y, Liu Y, Wang B, Mao J, Wang T, Ye K, Ye Y, Cram DS, Li H. Chen Y, et al. Prenat Diagn. 2016 Dec;36(13):1233-1241. doi: 10.1002/pd.4962. Epub 2016 Dec 9. Prenat Diagn. 2016. PMID: 27862068

6

A pregnancy with discordant fetal and placental chromosome 18 aneuploidies revealed by invasive and noninvasive prenatal diagnosis.

Chen C, Cram DS, Xie F, Wang P, Xu X, Li H, Song Z, Chen D, Zhang J, Tang S. Chen C, et al. Among authors: cram ds. Reprod Biomed Online. 2014 Jul;29(1):136-9. doi: 10.1016/j.rbmo.2014.03.017. Epub 2014 Apr 4. Reprod Biomed Online. 2014. PMID: 24797099

7

Feasibility of noninvasive prenatal testing for common fetal aneuploidies in an early gestational window.

Shi X, Zhang Z, Cram DS, Liu C. Shi X, et al. Clin Chim Acta. 2015 Jan 15;439:24-8. doi: 10.1016/j.cca.2014.09.032. Epub 2014 Oct 5. Clin Chim Acta. 2015. PMID: 25286007

8

The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities.

Li N, Wang L, Wang H, Ma M, Wang X, Li Y, Zhang W, Zhang J, Cram DS, Yao Y. Li N, et al. J Genet Genomics. 2015 Apr 20;42(4):151-9. doi: 10.1016/j.jgg.2015.03.001. Epub 2015 Mar 14. J Genet Genomics. 2015. PMID: 25953353

9

The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryos.

Fan J, Wang L, Wang H, Ma M, Wang S, Liu Z, Xu G, Zhang J, Cram DS, Yao Y. Fan J, et al. Reprod Biomed Online. 2015 Jul;31(1):62-70. doi: 10.1016/j.rbmo.2015.03.010. Epub 2015 Apr 9. Reprod Biomed Online. 2015. PMID: 25985995

10

Quantitation of fetal DNA fraction in maternal plasma using circulating single molecule amplification and re-sequencing technology (cSMART).

Song Y, Zhou X, Huang S, Li X, Qi Q, Jiang Y, Liu Y, Ma C, Li Z, Xu M, Cram DS, Liu J. Song Y, et al. Clin Chim Acta. 2016 May 1;456:151-156. doi: 10.1016/j.cca.2016.03.005. Epub 2016 Mar 15. Clin Chim Acta. 2016. PMID: 26993877

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