(Q50302069)

2 March 2018

title

Autism and maternally derived aberrations of chromosome 15q. (English)

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2 March 2018

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R J Schroer

1

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2 March 2018

M C Phelan

2

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2 March 2018

R C Michaelis

3

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2 March 2018

E C Crawford

4

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2 March 2018

S A Skinner

5

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2 March 2018

M Cuccaro

6

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2 March 2018

R J Simensen

7

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2 March 2018

J Bishop

8

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2 March 2018

C Skinner

9

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2 March 2018

D Fender

10

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2 March 2018

R E Stevenson

11

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2 March 2018

publication date

1 April 1998

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2 March 2018

American Journal of Medical Genetics Part A

published in

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2 March 2018

volume

76

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2 March 2018

page(s)

327-336

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2 March 2018

issue

4

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2 March 2018

Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.

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Autism as a strongly genetic disorder: evidence from a British twin study

21 January 2018

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

21 January 2018

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The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.

21 January 2018

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Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization

21 January 2018

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Forty four probands with an additional "marker" chromosome.

21 January 2018

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Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

21 January 2018

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Partial D 15 trisomy. A case and general review

21 January 2018

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Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosis.

21 January 2018

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Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

Autism associated with marker chromosome.

21 January 2018

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The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers

21 January 2018

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A case report of an autistic girl with an extra bisatellited marker chromosome

21 January 2018

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A case of autism associated with partial tetrasomy 15.

21 January 2018

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UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

1 reference

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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

1 reference

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Absence of predictable phenotypic expression in proximal 15q duplications

21 January 2018

1 reference

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Preferential maternal derivation in inv dup(15): analysis of eight new cases.

21 January 2018

1 reference

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De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

21 January 2018

1 reference

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Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?

21 January 2018

1 reference

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21 January 2018

1 reference

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Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

A bisatellited marker chromosome in a mentally retarded girl with infantile autism

21 January 2018

1 reference

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The UCLA-University of Utah epidemiologic survey of autism: the etiologic role of rare diseases

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

Autism and known medical conditions: myth and substance

21 January 2018

1 reference

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Intrachromosomal triplication of 15q11-q13.

21 January 2018

1 reference

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

21 January 2018

1 reference

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Autism in Angelman syndrome: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

Regression in pervasive developmental disorders: seizures and epileptiform electroencephalogram correlates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

Chromosome findings in twins with early-onset autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980401%2976%3A4%3C327%3A%3AAID-AJMG8%3E3.0.CO%3B2-M

10.1002/(SICI)1096-8628(19980401)76:4<327::AID-AJMG8>3.0.CO;2-M

21 January 2018

Identifiers

DOI

1 reference

2 March 2018

PubMed ID

9545097

1 reference

2 March 2018