(Q28283895)

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Autistic symptoms among children and young adults with isodicentric chromosome 15

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Autistic symptoms among children and young adults with isodicentric chromosome 15 (English)

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S Rineer

1

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B Finucane

series ordinal

2

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E W Simon

series ordinal

3

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language of work or name

English

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publication date

7 September 1998

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published in

American Journal of Medical Genetics Part A

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volume

81

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issue

5

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page(s)

428-33

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cites work

Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Forty four probands with an additional "marker" chromosome.

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Autism associated with marker chromosome.

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype

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reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome

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reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

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21 January 2018

Autistic disorder and additional inv dup(15)(pter----q13) chromosome.

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reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

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21 January 2018

Autism and maternally derived aberrations of chromosome 15q.

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https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

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21 January 2018

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

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https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Cytogenetic and clinical studies in five cases of inv dup(15)

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reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

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reference URL

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retrieved

21 January 2018

Autism associated with tetrasomy 15: A further report

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https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980907%2981%3A5%3C428%3A%3AAID-AJMG12%3E3.0.CO%3B2-E

retrieved

21 January 2018

Identifiers

DOI

10.1002/(SICI)1096-8628(19980907)81:5<428::AID-AJMG12>3.0.CO;2-E

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PubMed publication ID

9754629

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(Q28283895)

Autistic symptoms among children and young adults with isodicentric chromosome 15

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