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Items: 19

1.

Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.

Fonda Allen J, Stoll K, Bernhardt BA.

Semin Perinatol. 2016 Feb;40(1):44-55. doi: 10.1053/j.semperi.2015.11.007. Epub 2015 Dec 21. Review.

PMID:
26718445
2.

Genetic Counselors' Perspectives and Practices Regarding Expanded Carrier Screening after Initial Clinical Availability.

Lazarin GA, Detweiler S, Nazareth SB, Ashkinadze E.

J Genet Couns. 2016 Apr;25(2):395-404. doi: 10.1007/s10897-015-9881-1. Epub 2015 Sep 10.

3.

Women's Attitudes Regarding Prenatal Testing for a Range of Congenital Disorders of Varying Severity.

Norton ME, Nakagawa S, Kuppermann M.

J Clin Med. 2014 Jan 21;3(1):144-52. doi: 10.3390/jcm3010144.

4.

Changing trends in carrier screening for genetic disease in the United States.

Nazareth SB, Lazarin GA, Goldberg JD.

Prenat Diagn. 2015 Oct;35(10):931-5. doi: 10.1002/pd.4647. Epub 2015 Jul 27. Review.

5.

Preconception counseling: do patients learn about genetics from their obstetrician gynecologists?

Mandelberger AH, Robins JC, Buster JE, Strohsnitter WC, Plante BJ.

J Assist Reprod Genet. 2015 Jul;32(7):1145-9. doi: 10.1007/s10815-015-0491-5. Epub 2015 Jun 9.

6.

Obstetrician-gynecologists' knowledge of sickle cell disease screening and management.

Azonobi IC, Anderson BL, Byams VR, Grant AM, Schulkin J.

BMC Pregnancy Childbirth. 2014 Oct 14;14:356. doi: 10.1186/1471-2393-14-356.

7.

Sickle cell disease in pregnancy: maternal complications in a Medicaid-enrolled population.

Boulet SL, Okoroh EM, Azonobi I, Grant A, Craig Hooper W.

Matern Child Health J. 2013 Feb;17(2):200-7. doi: 10.1007/s10995-012-1216-3.

8.

"He didn't say that thalassaemia might come up" - β-thalassaemia carriers' experiences and attitudes.

Cousens NE, Gaff CL, Metcalfe SA, Delatycki MB.

J Community Genet. 2013 Apr;4(2):223-32. doi: 10.1007/s12687-012-0136-7. Epub 2013 Jan 13.

9.

An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals.

Lazarin GA, Haque IS, Nazareth S, Iori K, Patterson AS, Jacobson JL, Marshall JR, Seltzer WK, Patrizio P, Evans EA, Srinivasan BS.

Genet Med. 2013 Mar;15(3):178-86. doi: 10.1038/gim.2012.114. Epub 2012 Sep 13.

10.

Attitudes of general practitioners and midwives towards ethnicity-based haemoglobinopathy-carrier screening.

Jans SM, de Jonge A, Henneman L, Cornel MC, Lagro-Janssen AL.

Eur J Hum Genet. 2012 Nov;20(11):1112-7. doi: 10.1038/ejhg.2012.72. Epub 2012 May 2.

11.

Genomics and perinatal care.

Bodurtha J, Strauss JF 3rd.

N Engl J Med. 2012 Jan 5;366(1):64-73. doi: 10.1056/NEJMra1105043. Review. No abstract available.

12.

Genetic screening.

Burke W, Tarini B, Press NA, Evans JP.

Epidemiol Rev. 2011;33:148-64. doi: 10.1093/epirev/mxr008. Epub 2011 Jun 27. Review.

13.

Causes and mechanisms of intrauterine hypoxia and its impact on the fetal cardiovascular system: a review.

Hutter D, Kingdom J, Jaeggi E.

Int J Pediatr. 2010;2010:401323. doi: 10.1155/2010/401323. Epub 2010 Oct 19.

14.

Should bilateral uterine artery notching be used in the risk assessment for preeclampsia, small-for-gestational-age, and gestational hypertension?

Espinoza J, Kusanovic JP, Bahado-Singh R, Gervasi MT, Romero R, Lee W, Vaisbuch E, Mazaki-Tovi S, Mittal P, Gotsch F, Erez O, Gomez R, Yeo L, Hassan SS.

J Ultrasound Med. 2010 Jul;29(7):1103-15. Erratum in: J Ultrasound Med. 2010 Oct;29(10):1494.

15.

Carrier screening for beta-thalassaemia: a review of international practice.

Cousens NE, Gaff CL, Metcalfe SA, Delatycki MB.

Eur J Hum Genet. 2010 Oct;18(10):1077-83. doi: 10.1038/ejhg.2010.90. Epub 2010 Jun 23. Review.

16.

Evidence-based clinical guidelines for immigrants and refugees.

Pottie K, Greenaway C, Feightner J, Welch V, Swinkels H, Rashid M, Narasiah L, Kirmayer LJ, Ueffing E, MacDonald NE, Hassan G, McNally M, Khan K, Buhrmann R, Dunn S, Dominic A, McCarthy AE, Gagnon AJ, Rousseau C, Tugwell P; coauthors of the Canadian Collaboration for Immigrant and Refugee Health.

CMAJ. 2011 Sep 6;183(12):E824-925. doi: 10.1503/cmaj.090313. Epub 2010 Jun 7. No abstract available.

17.

Patient physical characteristics and primary care physician decision making in preconception genetic screening.

Bonham VL, Knerr S, Feero WG, Stevens N, Jenkins JF, McBride CM.

Public Health Genomics. 2010;13(6):336-44. doi: 10.1159/000262328. Epub 2009 Nov 26.

18.

Maternal knowledge and attitudes about newborn screening for sickle cell disease and cystic fibrosis.

Lang CW, Stark AP, Acharya K, Ross LF.

Am J Med Genet A. 2009 Nov;149A(11):2424-9. doi: 10.1002/ajmg.a.33074.

19.

Raising awareness of carrier testing for hereditary haemoglobinopathies in high-risk ethnic groups in the Netherlands: a pilot study among the general public and primary care providers.

Weinreich SS, de Lange-de Klerk ES, Rijmen F, Cornel MC, de Kinderen M, Plass AM.

BMC Public Health. 2009 Sep 15;9:338. doi: 10.1186/1471-2458-9-338.

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