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Deletion 2q syndrome?
scientific article published on 01 February 1988
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
title
Deletion 2q syndrome?
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
main subject
human chromosome 2
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3354619
retrieved
30 December 2022
chromosomal deletion syndrome
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3354619
retrieved
30 December 2022
author name string
Sánchez JM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
3354619
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=3354619
retrieved
30 December 2022
publication date
1 February 1988
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
full work available at URL
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320290231
1 reference
stated in
Crossref
DOI
10.1002/AJMG.1320290231
reference URL
https://api.crossref.org/works/10.1002/AJMG.1320290231
retrieved
30 December 2022
https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320290231
1 reference
stated in
Crossref
DOI
10.1002/AJMG.1320290231
reference URL
https://api.crossref.org/works/10.1002/AJMG.1320290231
retrieved
30 December 2022
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
volume
29
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
page(s)
453-456
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
cites work
Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33).
series ordinal
2
1 reference
stated in
Crossref
DOI
10.1002/AJMG.1320290231
reference URL
https://api.crossref.org/works/10.1002/AJMG.1320290231
retrieved
30 December 2022
Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation.
series ordinal
3
1 reference
stated in
Crossref
DOI
10.1002/AJMG.1320290231
reference URL
https://api.crossref.org/works/10.1002/AJMG.1320290231
retrieved
30 December 2022
Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22)
series ordinal
4
1 reference
stated in
Crossref
DOI
10.1002/AJMG.1320290231
reference URL
https://api.crossref.org/works/10.1002/AJMG.1320290231
retrieved
30 December 2022
A case of deletion 2q35----qter and a peculiar phenotype
series ordinal
5
1 reference
stated in
Crossref
DOI
10.1002/AJMG.1320290231
reference URL
https://api.crossref.org/works/10.1002/AJMG.1320290231
retrieved
30 December 2022
Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36).
series ordinal
8
1 reference
stated in
Crossref
DOI
10.1002/AJMG.1320290231
reference URL
https://api.crossref.org/works/10.1002/AJMG.1320290231
retrieved
30 December 2022
Identifiers
DOI
10.1002/AJMG.1320290231
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
PubMed ID
3354619
1 reference
stated in
Europe PubMed Central
PubMed ID
3354619
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3354619%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 September 2019
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