(Q51953579)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210320%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations (English)

1 reference

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12 November 2019

7

1 reference

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Regina Celia Mingroni Netto

12 November 2019

1

1 reference

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Ândrea Ribeiro-dos-santos

12 November 2019

5

1 reference

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12 November 2019

Francisco Mauro Salzano

8

object named as

Francisco M Salzano

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210320%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

10

A Magdalena Hurtado

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210320%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

author name string

Claudia B Angeli

2

1 reference

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12 November 2019

Maria Teresa B M Auricchio

3

1 reference

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12 November 2019

Emygdia R Leal-Mesquita

4

1 reference

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12 November 2019

Iris Ferrari

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210320%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Kim Hill

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210320%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Angela M Vianna-Morgante

11

1 reference

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12 November 2019

publication date

1 August 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12210320%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part A

12 November 2019

published in

1 reference

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12 November 2019

volume

111

1 reference

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12 November 2019

issue

3

1 reference

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12 November 2019

page(s)

243-252

1 reference

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The ancestry of Brazilian mtDNA lineages

12 November 2019

cites work

1 reference

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Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate

21 January 2018

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High resolution of human evolutionary trees with polymorphic microsatellites

21 January 2018

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21 January 2018

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The Wai Wai Indians of South America: history and genetics

21 January 2018

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Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan population

21 January 2018

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Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population

21 January 2018

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Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability.

21 January 2018

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

21 January 2018

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Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.

21 January 2018

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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

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Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation

21 January 2018

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Mitochondrial genome variation and the origin of modern humans

21 January 2018

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Population studies of the fragile X: a molecular approach

21 January 2018

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Origins and affinities of modern humans: a comparison of mitochondrial and nuclear genetic data

21 January 2018

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Microsatellite diversity and the demographic history of modern humans

21 January 2018

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The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data

21 January 2018

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Fragile X premutations are not a major cause of early menopause

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10572

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/10.1002%2FAJMG.10572

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10572

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/10.1002%2FAJMG.10572

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10572

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10572

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.10572

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

21 January 2018

1 reference

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Microsatellite data support an early population expansion in Africa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10572

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

21 January 2018

1 reference

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Advances in molecular analysis of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10572

A complex mutable polymorphism located within the fragile X gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10572