(Q50344992)

5 March 2018

title

Genetic and neurological evaluation in a sample of individuals with pervasive developmental disorders. (English)

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5 March 2018

author name string

Carlos Eduardo Steiner

series ordinal

1

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5 March 2018

Marilisa Mantovani Guerreiro

series ordinal

2

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5 March 2018

Antonia Paula Marques-de-Faria

series ordinal

3

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5 March 2018

publication date

9 June 2003

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5 March 2018

Arquivos de Neuro-Psiquiatria

published in

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5 March 2018

volume

61

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issue

2A

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page(s)

176-180

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Current Research Findings on Childhood Autism

cites work

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

The neurobiology of infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

Childhood autism: the need for physical investigations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

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/10.1590%2FS0004-282X2003000200003

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

Bilateral posterior parietal polymicrogyria: a mild form of congenital bilateral perisylvian syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

Macrocephaly, epilepsy, autism, dysmorphic features, and mental retardation in two sisters: a new autosomal recessive syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

Aberrant splicing of phenylalanine hydroxylase mRNA: The major cause for phenylketonuria in parts of southern Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

New evidence of cerebellar and brainstem hypoplasia in autistic infants, children and adolescents: The MR imaging study by Hashimoto and colleagues

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

Brain single-photon emission computed tomography for behavior disorders in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000200003

10.1590/S0004-282X2003000200003

21 January 2018

Identifiers

DOI

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5 March 2018

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5 March 2018