FMR1 gene mutation screening by TP-PCR in patients with premature ovarian failure and fragile-X. (Q44250695)

1 December 2017

title

FMR1 gene mutation screening by TP-PCR in patients with premature ovarian failure and fragile-X. (English)

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premature ovarian failure

1 December 2017

main subject

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Sengul Tural

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1 December 2017

Akın Tekcan

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1 December 2017

Nurten Kara

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1 December 2017

Mehmet Elbistan

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1 December 2017

Davut Güven

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1 December 2017

Haydar Ali Tasdemir

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1 December 2017

publication date

4 November 2014

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Gynecological Endocrinology

1 December 2017

published in

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1 December 2017

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1 December 2017

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1 December 2017

page(s)

191-195

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

1 December 2017

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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/10.3109%2F09513590.2014.975685

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

DNA methylation represses FMR-1 transcription in fragile X syndrome

21 January 2018

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Genetic aspects of premature ovarian failure: a literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Premature ovarian failure in the fragile X syndrome

21 January 2018

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Premature ovarian failure

21 January 2018

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

The pathophysiology of fragile x syndrome.

21 January 2018

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

The FMR1 premutation and reproduction

21 January 2018

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Premature ovarian failure with FMR1 premutation, X chromosome mosaicism and blood lymphocyte microchimerism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Fragile X syndrome: diagnostic and carrier testing

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Examination of reproductive aging milestones among women who carry the FMR1 premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Fragile X premutation screening in women with premature ovarian failure

21 January 2018

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Reproductive and menstrual history of females with fragile X expansions

21 January 2018

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Association of FMR1 repeat size with ovarian dysfunction

21 January 2018

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https://api.crossref.org/works/10.3109%2F09513590.2014.975685

The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2).

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Fragile X analysis of 1112 prenatal samples from 1991 to 2010.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Mosaicism for FMR1 gene full mutation and intermediate allele in a female foetus: a postzygotic retraction event.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insuffici

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

Fragile X premutations in familial premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590.2014.975685

10.3109/09513590.2014.975685

21 January 2018

Identifiers

DOI

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1 December 2017

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