Similar articles for PMID: 18200514

Year	Number of Results
1977	1
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1990	2
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2012	3
2013	1
2016	3
2017	1
2018	1
2019	1
2020	1
2022	1
2024	0

1

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

McConkie-Rosell A, Spiridigliozzi GA, Melvin E, Dawson DV, Lachiewicz AM. McConkie-Rosell A, et al. Am J Med Genet C Semin Med Genet. 2008 Feb 15;148C(1):56-69. doi: 10.1002/ajmg.c.30161. Am J Med Genet C Semin Med Genet. 2008. PMID: 18200514 Free PMC article.

2

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

McConkie-Rosell A, Heise EM, Spiridigliozzi GA. McConkie-Rosell A, et al. J Genet Couns. 2009 Aug;18(4):313-25. doi: 10.1007/s10897-009-9215-2. Epub 2009 Mar 11. J Genet Couns. 2009. PMID: 19277853 Free PMC article.

3

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. McConkie-Rosell A, et al. J Genet Couns. 2012 Feb;21(1):59-71. doi: 10.1007/s10897-011-9391-8. Epub 2011 Aug 9. J Genet Couns. 2012. PMID: 21826579 Free PMC article.

4

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

McConkie-Rosell A, Spiridigliozzi GA, Sullivan JA, Dawson DV, Lachiewicz AM. McConkie-Rosell A, et al. Am J Med Genet. 2000 Jun 19;92(5):336-42. doi: 10.1002/1096-8628(20000619)92:5<336::aid-ajmg8>3.0.co;2-l. Am J Med Genet. 2000. PMID: 10861663

5

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. Wehbe RM, et al. Am J Med Genet A. 2009 Jun;149A(6):1190-9. doi: 10.1002/ajmg.a.32840. Am J Med Genet A. 2009. PMID: 19449413 Free PMC article.

6

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

Anido A, Carlson LM, Sherman SL. Anido A, et al. J Genet Couns. 2007 Feb;16(1):97-104. doi: 10.1007/s10897-006-9049-0. Epub 2007 Feb 13. J Genet Couns. 2007. PMID: 17295053

7

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

McConkie-Rosell A, Spiridigliozzi GA, Iafolla T, Tarleton J, Lachiewicz AM. McConkie-Rosell A, et al. Am J Med Genet. 1997 Jan 10;68(1):62-9. doi: 10.1002/(sici)1096-8628(19970110)68:1<62::aid-ajmg12>3.0.co;2-m. Am J Med Genet. 1997. PMID: 8986278

8

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

Curtis G, Dennis N, MacPherson J. Curtis G, et al. J Med Genet. 1994 Dec;31(12):950-2. doi: 10.1136/jmg.31.12.950. J Med Genet. 1994. PMID: 7891377 Free PMC article.

9

Fragile X screening program in a Spanish region.

Gabarrón J, Lopez I, Glover G, Carbonell P. Gabarrón J, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):333-8. doi: 10.1002/ajmg.1320430151. Am J Med Genet. 1992. PMID: 1605207

10

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. McConkie-Rosell A, et al. Am J Med Genet. 2001 Jan 1;98(1):37-45. Am J Med Genet. 2001. PMID: 11426454

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