A systematic review of population screening for fragile X syndrome (Q37765126)

22 August 2017

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title

A systematic review of population screening for fragile X syndrome (English)

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22 August 2017

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Melissa K Hill

1

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22 August 2017

Alison D Archibald

series ordinal

2

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22 August 2017

Jonathan Cohen

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3

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22 August 2017

Sylvia A Metcalfe

series ordinal

4

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22 August 2017

language of work or name

English

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publication date

1 July 2010

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22 August 2017

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22 August 2017

12

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22 August 2017

7

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22 August 2017

396-410

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https://scigraph.springernature.com/pub.10.1097/gim.0b013e3181e38fb6

22 August 2017

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Screening with the FMR1 protein test among mentally retarded males.

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FMR1 and the fragile X syndrome: human genome epidemiology review

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Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

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21 January 2018

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21 January 2018

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21 January 2018

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A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Cost-effectiveness analysis of prenatal population-based fragile X carrier screening

21 January 2018

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Economic evaluation of prenatal population screening for fragile X syndrome.

21 January 2018

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Incidence of fragile X in 5,000 consecutive newborn males.

21 January 2018

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

21 January 2018

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

21 January 2018

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Emotional reaction to fragile X premutation carrier tests among infertile women

21 January 2018

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10.1097/GIM.0B013E3181E38FB6

21 January 2018

Identifiers

DOI

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Dimensions Publication ID

22 August 2017

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1 reference