(Q33970872)

30 July 2017

1 reference

title

Three probands with autistic disorder and isodicentric chromosome 15. (English)

1 reference

30 July 2017

0 references

Wolpert CM

1

1 reference

30 July 2017

Menold MM

2

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30 July 2017

Bass MP

3

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30 July 2017

Qumsiyeh MB

4

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30 July 2017

Donnelly SL

5

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30 July 2017

Ravan SA

6

1 reference

30 July 2017

Vance JM

7

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30 July 2017

Gilbert JR

8

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30 July 2017

Abramson RK

9

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30 July 2017

Wright HH

10

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30 July 2017

Cuccaro ML

11

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30 July 2017

Pericak-Vance MA

12

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30 July 2017

1 June 2000

1 reference

American Journal of Medical Genetics Part A

30 July 2017

1 reference

30 July 2017

96

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30 July 2017

365-372

1 reference

30 July 2017

3

1 reference

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

30 July 2017

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

A case-control family history study of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Brief report: epidemiology of autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Maladaptive behavior in children with Prader-Willi syndrome, Down syndrome, and nonspecific mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

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%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Infantile autism: a genetic study of 21 twin pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Autism associated with marker chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

A case of autism associated with partial tetrasomy 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

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

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Is Angelman syndrome an alternate result of del(15)(q11q13)?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Hypomelanosis of ITO. A study of 76 infantile cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Concordance for the syndrome of autism in 40 pairs of afflicted twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Oculocutaneous albinism and mental disorder. A report of two autistic boys

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Genetic factors in child psychiatric disorders--I. A review of research strategies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Genetic factors in child psychiatric disorders--II. Empirical findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Autism and genetics. A decade of research

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Autism in Angelman syndrome: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Behaviour problems in Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Polygenic disease: methods for mapping complex disease traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000612%2996%3A3%3C365%3A%3AAID-AJMG25%3E3.0.CO%3B2-X

10.1002/1096-8628(20000612)96:3<365::AID-AJMG25>3.0.CO;2-X

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference