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Items: 1 to 20 of 105

1.

When to tell and test for genetic carrier status: perspectives of adolescents and young adults from fragile X families.

Wehbe RM, Spiridigliozzi GA, Heise EM, Dawson DV, McConkie-Rosell A.

Am J Med Genet A. 2009 Jun;149A(6):1190-9. doi: 10.1002/ajmg.a.32840.

2.

Genetic risk communication: experiences of adolescent girls and young women from families with fragile X syndrome.

McConkie-Rosell A, Heise EM, Spiridigliozzi GA.

J Genet Couns. 2009 Aug;18(4):313-25. doi: 10.1007/s10897-009-9215-2. Epub 2009 Mar 11.

3.

Longitudinal study of the carrier testing process for fragile X syndrome: perceptions and coping.

McConkie-Rosell A, Spiridigliozzi GA, Sullivan JA, Dawson DV, Lachiewicz AM.

Am J Med Genet. 2001 Jan 1;98(1):37-45.

PMID:
11426454
4.

Carrier testing in fragile X syndrome: when to tell and test.

McConkie-Rosell A, Spiridigliozzi GA, Sullivan JA, Dawson DV, Lachiewicz AM.

Am J Med Genet. 2002 Jun 1;110(1):36-44.

PMID:
12116269
5.

Influence of genetic risk information on parental role identity in adolescent girls and young women from families with fragile X syndrome.

McConkie-Rosell A, Heise EM, Spiridigliozzi GA.

J Genet Couns. 2012 Feb;21(1):59-71. doi: 10.1007/s10897-011-9391-8. Epub 2011 Aug 9.

6.

Carrier testing in the fragile X syndrome: attitudes and opinions of obligate carriers.

McConkie-Rosell A, Spiridigliozzi GA, Iafolla T, Tarleton J, Lachiewicz AM.

Am J Med Genet. 1997 Jan 10;68(1):62-9.

PMID:
8986278
7.

"It's something I need to consider": decisions about carrier screening for fragile X syndrome in a population of non-pregnant women.

Archibald AD, Jaques AM, Wake S, Collins VR, Cohen J, Metcalfe SA.

Am J Med Genet A. 2009 Dec;149A(12):2731-8. doi: 10.1002/ajmg.a.33122.

PMID:
19938084
8.

Benefits and burdens of genetic carrier identification.

Williams JK, Schutte DL.

West J Nurs Res. 1997 Feb;19(1):71-81.

PMID:
9030039
9.

Communication of genetic risk information to daughters in families with fragile X syndrome: the parent's perspective.

McConkie-Rosell A, Del Giorno J, Heise EM.

J Genet Couns. 2011 Feb;20(1):58-69. doi: 10.1007/s10897-010-9326-9. Epub 2010 Sep 28.

10.

Attitudes toward fragile X mutation carrier testing from women identified in a general population survey.

Anido A, Carlson LM, Sherman SL.

J Genet Couns. 2007 Feb;16(1):97-104. Epub 2007 Feb 13.

PMID:
17295053
11.

Carrier testing in fragile X syndrome: effect on self-concept.

McConkie-Rosell A, Spiridigliozzi GA, Sullivan JA, Dawson DV, Lachiewicz AM.

Am J Med Genet. 2000 Jun 19;92(5):336-42.

PMID:
10861663
12.

Living with genetic risk: effect on adolescent self-concept.

McConkie-Rosell A, Spiridigliozzi GA, Melvin E, Dawson DV, Lachiewicz AM.

Am J Med Genet C Semin Med Genet. 2008 Feb 15;148C(1):56-69. doi: 10.1002/ajmg.c.30161.

13.

Women's attitudes toward testing for fragile X carrier status: a qualitative analysis.

Anido A, Carlson LM, Taft L, Sherman SL.

J Genet Couns. 2005 Aug;14(4):295-306.

PMID:
16047092
14.

DNA testing for fragile X syndrome in schools for learning difficulties.

Slaney SF, Wilkie AO, Hirst MC, Charlton R, McKinley M, Pointon J, Christodoulou Z, Huson SM, Davies KE.

Arch Dis Child. 1995 Jan;72(1):33-7.

15.

Carrier diagnosis of the fragile X syndrome--a challenge in antenatal clinics.

Ryynänen M, Kirkinen P, Mannermaa A, Saarikoski S.

Am J Obstet Gynecol. 1995 Apr;172(4 Pt 1):1236-9.

PMID:
7726262
16.

Levels and associations among self-esteem, fertility distress, coping, and reaction to potentially being a genetic carrier in women with diminished ovarian reserve.

Cizmeli C, Lobel M, Franasiak J, Pastore LM.

Fertil Steril. 2013 Jun;99(7):2037-44.e3. doi: 10.1016/j.fertnstert.2013.02.033. Epub 2013 Mar 15.

17.

"It's about having the choice": stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome.

Archibald AD, Hickerton CL, Jaques AM, Wake S, Cohen J, Metcalfe SA.

Am J Med Genet A. 2013 Jan;161A(1):48-58. doi: 10.1002/ajmg.a.35674. Epub 2012 Dec 13.

PMID:
23239566
18.

A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study.

Metcalfe S, Jacques A, Archibald A, Burgess T, Collins V, Henry A, McNamee K, Sheffield L, Slater H, Wake S, Cohen J.

Genet Med. 2008 Jul;10(7):525-35. doi: 10.1097GIM.0b013e31817c036e.

PMID:
18580686
19.

DNA testing for fragile X syndrome: implications for parents and family.

van Rijn MA, de Vries BB, Tibben A, van den Ouweland AM, Halley DJ, Niermeijer MF.

J Med Genet. 1997 Nov;34(11):907-11.

20.

The impact of genetic counselling on females in fragile X families.

Curtis G, Dennis N, MacPherson J.

J Med Genet. 1994 Dec;31(12):950-2.

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