(Q77759362)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10331590%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

Fully mutated and gray-zone FRAXA alleles in Brazilian mentally retarded boys (English)

1 reference

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Regina Celia Mingroni Netto

8 December 2019

author

4

1 reference

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8 December 2019

author name string

L A Haddad

1

1 reference

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8 December 2019

M J Aguiar

2

1 reference

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8 December 2019

S S Costa

3

1 reference

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8 December 2019

A M Vianna-Morgante

5

1 reference

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8 December 2019

S D Pena

6

1 reference

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8 December 2019

publication date

1 May 1999

1 reference

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American Journal of Medical Genetics Part A

8 December 2019

published in

1 reference

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8 December 2019

volume

84

1 reference

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8 December 2019

issue

3

1 reference

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8 December 2019

page(s)

198-201

1 reference

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

8 December 2019

cites work

1 reference

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Simultaneous detection of size and sequence polymorphisms in the transcribed trinucleotide repeat D2S196E (EST00493).

21 January 2018

1 reference

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CAT repeat polymorphism in a human expressed sequence tag (EST00444) (D13S308).

21 January 2018

1 reference

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Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing.

21 January 2018

1 reference

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Population studies of the fragile X: a molecular approach

21 January 2018

1 reference

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Relationship of expansion of CGG repeats and X-inactivation with expression of fra(X)(q27.3) in heterozygotes

21 January 2018

1 reference

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Fragile X frequency in a mentally retarded population in Brazil.

21 January 2018

1 reference

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An n-allele model for progressive amplification in the FMR1 locus

21 January 2018

1 reference

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Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.

21 January 2018

1 reference

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DNA bioprints: simple nonisotopic DNA fingerprints with biotinylated probes

21 January 2018

1 reference

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Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990528%2984%3A3%3C198%3A%3AAID-AJMG5%3E3.0.CO%3B2-W

Genetic and population study of a Y-linked tetranucleotide repeat DNA polymorphism with a simple non-isotopic technique

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990528%2984%3A3%3C198%3A%3AAID-AJMG5%3E3.0.CO%3B2-W

Prevalence of fragile X syndrome

21 January 2018

1 reference

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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/10.1002%2F%28SICI%291096-8628%2819990528%2984%3A3%3C198%3A%3AAID-AJMG5%3E3.0.CO%3B2-W

10.1002/(SICI)1096-8628(19990528)84:3<198::AID-AJMG5>3.0.CO;2-W

21 January 2018

Identifiers

DOI

1 reference

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8 December 2019

1 reference