(Q50307094)

English

Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports.

scientific article published in December 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

0 references

autism spectrum disorder

0 references

object named as

Mima Simic

1

0 references

author name string

Jeremy Turk

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

publication date

1 December 2004

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

European Child & Adolescent Psychiatry

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

13

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

389-393

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

https://scigraph.springernature.com/pub.10.1007/s00787-004-0414-y

0 references

Psychological characteristics of Turner syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and molecular analysis of five inv dup(15) patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effect

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescencein situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal origin of inv dup(15) chromosomes in infantile autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and tuberous sclerosis complex: prevalence and clinical features

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and maternally derived aberrations of chromosome 15q.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenylketonuria: mental development, behavior, and termination of low phenylalanine diet.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychiatric disorder among children with tuberous sclerosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal disorders and autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angelman syndrome: evolution of the phenotype in adolescents and adults.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic studies in autistic disorder and chromosome 15.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15619052

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00787-004-0414-Y

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15619052

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