(Q34722075)

4 August 2017

A single-tube quantitative high-resolution melting curve method for parent-of-origin determination of 15q duplications (English)

1 reference

4 August 2017

3

Edwin H Cook

1 reference

4 August 2017

Nora Urraca

1

1 reference

4 August 2017

Lea Davis

series ordinal

2

1 reference

4 August 2017

N Carolyn Schanen

series ordinal

4

1 reference

4 August 2017

Lawrence T Reiter

series ordinal

5

1 reference

4 August 2017

1 August 2010

1 reference

Genetic Testing and Molecular Biomarkers

4 August 2017

1 reference

4 August 2017

14

1 reference

4 August 2017

4

1 reference

4 August 2017

571-576

1 reference

Meta-Analysis of Early Intensive Behavioral Intervention for Children With Autism

4 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

Early behavioral intervention, brain plasticity, and the prevention of autism spectrum disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

Early communication development and intervention for children with autism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

Mechanisms of imprinting of the Prader-Willi/Angelman region.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3064527

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

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20642357

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Methylation-Sensitive High-Resolution Melting-Curve Analysis of the SNRPN Gene as a Diagnostic Screen for Prader-Willi and Angelman Syndromes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20642357

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1089/GTMB.2010.0030

1 reference

4 August 2017

1 reference

4 August 2017

1 reference