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Items: 1 to 20 of 128

1.

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.

J Genet Couns. 2014 Dec;23(6):1012-21. doi: 10.1007/s10897-014-9725-4. Epub 2014 May 3.

PMID:
24788196
2.

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.

Am J Med Genet A. 2013 Jul;161A(7):1612-8. doi: 10.1002/ajmg.a.35972. Epub 2013 May 21.

PMID:
23696422
3.

An easy test but a hard decision: ethical issues concerning non-invasive prenatal testing for autosomal recessive disorders.

Skirton H, Goldsmith L, Chitty LS.

Eur J Hum Genet. 2015 Aug;23(8):1004-9. doi: 10.1038/ejhg.2014.238. Epub 2014 Nov 5.

4.

Effectiveness of earlier antenatal screening for sickle cell disease and thalassaemia in primary care: cluster randomised trial.

Dormandy E, Gulliford M, Bryan S, Roberts TE, Calnan M, Atkin K, Karnon J, Logan J, Kavalier F, Harris HJ, Johnston TA, Anionwu EN, Tsianakas V, Jones P, Marteau TM.

BMJ. 2010 Oct 5;341:c5132. doi: 10.1136/bmj.c5132.

5.

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.

Hussein N, Weng SF, Kai J, Kleijnen J, Qureshi N.

Cochrane Database Syst Rev. 2015 Aug 12;(8):CD010849. doi: 10.1002/14651858.CD010849.pub2. Review.

PMID:
26264938
6.

Counselling for prenatal diagnosis of sickle cell disease and beta thalassaemia major: a four year experience.

Anionwu EN, Patel N, Kanji G, Renges H, Brozović M.

J Med Genet. 1988 Nov;25(11):769-72.

7.

Impact of fetal or child loss on parents' perceptions of non-invasive prenatal diagnosis for autosomal recessive conditions.

Pisnoli L, O'Connor A, Goldsmith L, Jackson L, Skirton H.

Midwifery. 2016 Mar;34:105-10. doi: 10.1016/j.midw.2015.12.009. Epub 2016 Jan 1.

PMID:
26821974
8.
9.

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

Lewis C, Hill M, Chitty LS.

Clin Genet. 2014 Apr;85(4):336-42. doi: 10.1111/cge.12179. Epub 2013 May 27.

PMID:
23631435
10.

Prenatal diagnosis of sickle syndromes in India: dilemmas in counselling.

Colah R, Surve R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Satoskar P, Mohanty D.

Prenat Diagn. 2005 May;25(5):345-9.

PMID:
15906420
11.

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.

Haemophilia. 2012 Jul;18(4):575-83. doi: 10.1111/j.1365-2516.2011.02653.x. Epub 2011 Sep 23.

PMID:
21951674
12.

Offering antenatal sickle cell and thalassaemia screening to pregnant women in primary care: a qualitative study of GPs' experiences.

Tsianakas V, Calnan M, Atkin K, Dormandy E, Marteau TM.

Br J Gen Pract. 2010 Nov;60(580):822-8. doi: 10.3399/bjgp10X532602.

13.

Will the introduction of non-invasive prenatal diagnostic testing erode informed choices? An experimental study of health care professionals.

van den Heuvel A, Chitty L, Dormandy E, Newson A, Deans Z, Attwood S, Haynes S, Marteau TM.

Patient Educ Couns. 2010 Jan;78(1):24-8. doi: 10.1016/j.pec.2009.05.014. Epub 2009 Jun 26.

PMID:
19560305
14.

Non-invasive prenatal diagnosis (NIPD) for single gene disorders: cost analysis of NIPD and invasive testing pathways.

Verhoef TI, Hill M, Drury S, Mason S, Jenkins L, Morris S, Chitty LS.

Prenat Diagn. 2016 Jul;36(7):636-42. doi: 10.1002/pd.4832. Epub 2016 May 22.

PMID:
27107169
16.

Changing their minds with time: a comparison of hypothetical and actual reproductive behaviors in parents of children with cystic fibrosis.

Sawyer SM, Cerritelli B, Carter LS, Cooke M, Glazner JA, Massie J.

Pediatrics. 2006 Sep;118(3):e649-56.

PMID:
16950956
17.

Ethical aspects arising from non-invasive fetal diagnosis.

Newson AJ.

Semin Fetal Neonatal Med. 2008 Apr;13(2):103-8. doi: 10.1016/j.siny.2007.12.004. Review.

PMID:
18243828
18.

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

Lewis C, Hill M, Skirton H, Chitty LS.

Eur J Hum Genet. 2012 Nov;20(11):1127-33. doi: 10.1038/ejhg.2012.50. Epub 2012 Mar 28.

19.

Prepregnancy testing for single-gene disorders by polar body analysis.

Verlinsky Y, Rechitsky S, Verlinsky O, Ivachnenko V, Lifchez A, Kaplan B, Moise J, Valle J, Borkowski A, Nefedova J, Goltsman E, Strom C, Kuliev A.

Genet Test. 1999;3(2):185-90.

PMID:
10464666
20.

Prenatal diagnosis of hemoglobinopathies.

Fischel-Ghodsian N.

Clin Perinatol. 1990 Dec;17(4):811-28. Review.

PMID:
2286030

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