Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q38365109)
Watch
English
A clinical case report and literature review of the 3q29 microdeletion syndrome.
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
review article
1 reference
stated in
Europe PubMed Central
title
A clinical case report and literature review of the 3q29 microdeletion syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
author
Devin M Cox
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
author name string
Merlin G Butler
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
publication date
1 July 2015
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
published in
Clinical Dysmorphology
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
volume
24
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
issue
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
page(s)
89-94
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
cites work
A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
6 September 2017
The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
6 September 2017
Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
6 September 2017
A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
6 September 2017
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
6 September 2017
Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
6 September 2017
The 3q29 microdeletion syndrome: report of three new unrelated patients and in silico "RNA binding" analysis of the 3q29 region.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
1.6Mb deletion in chromosome band 3q29 associated with eye abnormalities.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
31 August 2018
Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
5 November 2018
3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5125389
retrieved
3 December 2018
Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25714563
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1097/MCD.0000000000000077
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
PMC publication ID
5125389
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
PubMed publication ID
25714563
1 reference
stated in
Europe PubMed Central
PMC publication ID
5125389
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25714563%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
