(Q52105468)

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Genetic and clinical characterization of patients with an interstitial duplication 15q11‐q13, emphasizing behavioral phenotype and response to treatment

scientific article published on June 1, 2003

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scholarly article

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/12749048

Genetic and clinical characterization of patients with an interstitial duplication 15q11‐q13, emphasizing behavioral phenotype and response to treatment (English)

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most precise value

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12749048

2 January 2024

1 reference

10.1002/AJMG.A.10176

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2 January 2024

Nicole Tartaglia

5

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N. Tartaglia

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2 January 2024

author name string

LeRoux J

6

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Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/12749048

J. A. Thomas

1

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2 January 2024

J. Johnson

2

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2 January 2024

T. L. Peterson Kraai

3

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2 January 2024

R. Wilson

4

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2 January 2024

J. LeRoux

6

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2 January 2024

L. Beischel

7

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2 January 2024

L. McGavran

8

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2 January 2024

R. J. Hagerman

9

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2 January 2024

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publication date

1 June 2003

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22 April 2018

http://europepmc.org/abstract/MED/12749048

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https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.a.10176

1 reference

10.1002/AJMG.A.10176

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2 January 2024

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.10176

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2 January 2024

American Journal of Medical Genetics

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http://europepmc.org/abstract/MED/12749048

119A

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http://europepmc.org/abstract/MED/12749048

111-120

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http://europepmc.org/abstract/MED/12749048

2

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Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/12749048

Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR)

1

1 reference

10.1002/AJMG.A.10176

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2 January 2024

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

2

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

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

3

1 reference

10.1002/AJMG.A.10176

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2 January 2024

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

4

1 reference

10.1002/AJMG.A.10176

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2 January 2024

Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome

5

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

A new self-report scale for assessment of adolescent psychopathology: factor structure, reliability, validity, and diagnostic sensitivity.

6

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

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

7

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Effects of fluoxetine treatment in young children with idiopathic autism.

8

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

9

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

10

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Form of 15q proximal duplication appears to be a normal euchromatic variant

12

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome

14

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Absence of predictable phenotypic expression in proximal 15q duplications

15

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

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

17

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.

20

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

The evaluation of 15q proximal duplications by FISH

21

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications.

22

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Autism and maternally derived aberrations of chromosome 15q.

24

1 reference

10.1002/AJMG.A.10176

https://api.crossref.org/works/10.1002/AJMG.A.10176

2 January 2024

Identifiers

10.1002/AJMG.A.10176

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/12749048

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/12749048

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