(Q35804773)

10 August 2017

0 references

Tetrasomy 15q11-q13 diagnosed by FISH in a patient with autistic disorder (English)

1 reference

10 August 2017

0 references

Karim Ouldim

1

1 reference

10 August 2017

Abdelhafid Natiq

series ordinal

2

1 reference

10 August 2017

Philippe Jonveaux

series ordinal

3

1 reference

10 August 2017

Abdelaziz Sefiani

series ordinal

4

1 reference

10 August 2017

language of work or name

1 reference

20 March 2007

1 reference

Journal of Biomedicine and Biotechnology

10 August 2017

1 reference

10 August 2017

2007

1 reference

10 August 2017

3

1 reference

10 August 2017

61538

1 reference

Creative Commons Attribution 3.0 Unported

10 August 2017

start time

1 January 2007

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

describes a project that uses

fluorescence in situ hybridization

1 reference

based on heuristic

inferred from title

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

Molecular genetics of autism spectrum disorder.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

11 July 2018

The genetics of autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

Molecular and Fluorescence In Situ Hybridization Characterization of the Breakpoints in 46 Large Supernumerary Marker 15 Chromosomes Reveals an Unexpected Level of Complexity

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

Three probands with autistic disorder and isodicentric chromosome 15.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

The origin and behavior of two isodicentric bisatellited chromosomes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

Chromosomal disorders and autism.

11 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1155%2F2007%2F61538

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1155%2F2007%2F61538

Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1874673

25 September 2018

Identifiers

DOI

10.1155/2007/61538

1 reference

10 August 2017

1 reference

10 August 2017

1 reference