(Q38331560)

2 September 2017

title

CGG repeat interruptions in the FMR1 gene in patients with infantile autism (English)

1 reference

2 September 2017

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P M Poon

1

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2 September 2017

Q L Chen

2

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2 September 2017

K Y Lai

3

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2 September 2017

C K Wong

4

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2 September 2017

C P Pang

5

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2 September 2017

publication date

1 August 1998

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Clinical Chemistry and Laboratory Medicine

2 September 2017

published in

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2 September 2017

volume

36

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2 September 2017

issue

8

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2 September 2017

page(s)

649-653

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The fragile X syndrome II: preliminary data on growth and development in males

2 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

An analysis of autism in fifty males with the fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

Autism is associated with the fragile-X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

Fine structure of the human FMR1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

Fragile X founder effects and new mutations in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.1998.115

21 January 2018

Identifiers

DOI

10.1515/CCLM.1998.115

1 reference

2 September 2017

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