Cram DS - Search Results

1

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. Among authors: cram ds. 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

2

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. 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

3

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. Among authors: cram ds. Prenat Diagn. 2016 Dec;36(13):1233-1241. doi: 10.1002/pd.4962. Epub 2016 Dec 9. Prenat Diagn. 2016. PMID: 27862068

4

Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia Carriers.

Xu L, Mao A, Liu H, Gui B, Choy KW, Huang H, Yu Q, Zhang X, Chen M, Lin N, Chen L, Han J, Wang Y, Zhang M, Li X, He D, Lin Y, Zhang J, Cram DS, Cao H. Xu L, et al. Among authors: cram ds. J Mol Diagn. 2020 Aug;22(8):1087-1095. doi: 10.1016/j.jmoldx.2020.05.004. Epub 2020 May 29. J Mol Diagn. 2020. PMID: 32473995 Free article.

5

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. Among authors: cram ds. 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

6

Potential of syncytiotrophoblasts isolated from the cervical mucus for early non-invasive prenatal diagnosis: evidence of a vanishing twin.

Mantzaris D, Cram DS. Mantzaris D, et al. Among authors: cram ds. Clin Chim Acta. 2015 Jan 1;438:309-15. doi: 10.1016/j.cca.2014.09.002. Epub 2014 Sep 8. Clin Chim Acta. 2015. PMID: 25218787

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. Among authors: cram ds. 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

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. Among authors: cram ds. 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

9

A comparative study of EGFR oncogenic mutations in matching tissue and plasma samples from patients with advanced non-small cell lung carcinoma.

Chai X, Ren P, Wei B, Ma J, Mai L, Cram DS, Song Y, Guo Y. Chai X, et al. Among authors: cram ds. Clin Chim Acta. 2016 Jun 1;457:106-11. doi: 10.1016/j.cca.2016.04.003. Epub 2016 Apr 9. Clin Chim Acta. 2016. PMID: 27071701

10

A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree.

Xue J, Gao Q, Huang Y, Zhang X, Yang P, Cram DS, Liang D, Wu L. Xue J, et al. Among authors: cram ds. Clin Chim Acta. 2016 Oct 1;461:135-40. doi: 10.1016/j.cca.2016.07.025. Epub 2016 Jul 30. Clin Chim Acta. 2016. PMID: 27485761

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