(Q52117346)

22 April 2018

title

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

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22 April 2018

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Allyn McConkie-Rosell

1

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22 April 2018

Gail A Spiridigliozzi

2

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22 April 2018

Jennifer A Sullivan

3

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22 April 2018

Deborah V Dawson

4

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22 April 2018

Ave M Lachiewicz

5

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22 April 2018

publication date

1 June 2002

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22 April 2018

American Journal of Medical Genetics Part A

published in

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22 April 2018

volume

110

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22 April 2018

issue

1

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22 April 2018

page(s)

36-44

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22 April 2018

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

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1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

Huntington's disease predictive testing: the case for an assessment approach to requests from adolescents

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Barriers to carrier testing for adult cystic fibrosis sibs: the importance of not knowing

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Dissemination of genetic risk information to relatives in the fragile X syndrome: guidelines for genetic counselors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

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

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

Genetic Counseling for Fragile X Syndrome: Recommendations of the National Society of Genetic Counselors

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

21 January 2018

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Genetic testing for children and adolescents. Who decides?

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Predictive genetic testing in children: The need for psychological research

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Testing Adolescents for a Hereditary Breast Cancer Gene (BRCA1)

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10396

Attitudes toward the genetic testing of children among adults in a Utah-based kindred tested for a BRCA1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

Parental attitudes regarding carrier testing in children at risk for fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

Prevalence of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

A private view of heterozygosity: eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10396

21 January 2018

Identifiers

DOI

10.1002/AJMG.10396

1 reference

22 April 2018

1 reference

22 April 2018