Lewis C - Search Results

1

Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals.

Lewis C, Hammond J, Klapwijk JE, Harding E, Lou S, Vogel I, Szepe EJ, Hui L, Ingvoldstad-Malmgren C, Soller MJ, Ormond KE, Choolani M, Hill M, Riedijk S. Lewis C, et al. Prenat Diagn. 2021 May;41(6):720-732. doi: 10.1002/pd.5932. Epub 2021 Mar 30. Prenat Diagn. 2021. PMID: 33724493 Free PMC article.

2

Determination of foetal sex in pregnancies at risk of haemophilia: a qualitative study exploring the clinical practices and attitudes of health professionals in the United Kingdom.

Hill M, Compton C, Lewis C, Skirton H, Chitty LS. Hill M, et al. Among authors: lewis c. Haemophilia. 2012 Jul;18(4):575-83. doi: 10.1111/j.1365-2516.2011.02653.x. Epub 2011 Sep 23. Haemophilia. 2012. PMID: 21951674

3

Non-invasive prenatal diagnosis for fetal sex determination: benefits and disadvantages from the service users' perspective.

Lewis C, Hill M, Skirton H, Chitty LS. Lewis C, et al. Eur J Hum Genet. 2012 Nov;20(11):1127-33. doi: 10.1038/ejhg.2012.50. Epub 2012 Mar 28. Eur J Hum Genet. 2012. PMID: 22453293 Free PMC article.

4

Implementing noninvasive prenatal fetal sex determination using cell-free fetal DNA in the United Kingdom.

Hill M, Lewis C, Jenkins L, Allen S, Elles RG, Chitty LS. Hill M, et al. Among authors: lewis c. Expert Opin Biol Ther. 2012 Jun;12 Suppl 1:S119-26. doi: 10.1517/14712598.2012.666522. Epub 2012 Apr 16. Expert Opin Biol Ther. 2012. PMID: 22500945

5

Fetal sex determination using cell-free fetal DNA: service users' experiences of and preferences for service delivery.

Lewis C, Hill M, Skirton H, Chitty LS. Lewis C, et al. Prenat Diagn. 2012 Aug;32(8):735-41. doi: 10.1002/pd.3893. Epub 2012 May 10. Prenat Diagn. 2012. PMID: 22573474

6

Non-invasive prenatal testing for single gene disorders: exploring the ethics.

Deans Z, Hill M, Chitty LS, Lewis C. Deans Z, et al. Among authors: lewis c. Eur J Hum Genet. 2013 Jul;21(7):713-8. doi: 10.1038/ejhg.2012.250. Epub 2012 Nov 28. Eur J Hum Genet. 2013. PMID: 23188047 Free PMC article.

7

Non-invasive prenatal diagnosis for single gene disorders: experience of patients.

Lewis C, Hill M, Chitty LS. Lewis C, et al. Clin Genet. 2014 Apr;85(4):336-42. doi: 10.1111/cge.12179. Epub 2013 May 27. Clin Genet. 2014. PMID: 23631435

8

Views and preferences for the implementation of non-invasive prenatal diagnosis for single gene disorders from health professionals in the United Kingdom.

Hill M, Karunaratna M, Lewis C, Forya F, Chitty L. Hill M, et al. Among authors: lewis c. Am J Med Genet A. 2013 Jul;161A(7):1612-8. doi: 10.1002/ajmg.a.35972. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696422

9

Non-invasive prenatal testing for trisomy 21: a cross-sectional survey of service users' views and likely uptake.

Lewis C, Hill M, Silcock C, Daley R, Chitty LS. Lewis C, et al. BJOG. 2014 Apr;121(5):582-94. doi: 10.1111/1471-0528.12579. Epub 2014 Jan 17. BJOG. 2014. PMID: 24433394

10

Client views and attitudes to non-invasive prenatal diagnosis for sickle cell disease, thalassaemia and cystic fibrosis.

Hill M, Compton C, Karunaratna M, Lewis C, Chitty L. Hill M, et al. Among authors: lewis c. J Genet Couns. 2014 Dec;23(6):1012-21. doi: 10.1007/s10897-014-9725-4. Epub 2014 May 3. J Genet Couns. 2014. PMID: 24788196

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