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English
The last shall be first
scientific article published on 01 February 1993
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
title
The last shall be first
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
author name string
Trent JM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
Meltzer PS
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
publication date
1 February 1993
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
volume
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
page(s)
101-102
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
cites work
Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
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inferred from DOI database lookup
Translocations, master genes, and differences between the origins of acute and chronic leukemias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome aberrations and cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning: let's not call it reverse anymore
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
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Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0293-101
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0293-101
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
PubMed publication ID
8499942
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8499942
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8499942%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
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