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Single-minded and Down syndrome?
scientific article
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instance of
scholarly article
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title
Single-minded and Down syndrome?
(English)
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author
Roman Chrast
object named as
R Chrast
series ordinal
2
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author name string
H Chen
series ordinal
1
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C Rossier
series ordinal
3
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A Gos
series ordinal
4
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S E Antonarakis
series ordinal
5
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J Kudoh
series ordinal
6
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A Yamaki
series ordinal
7
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N Shindoh
series ordinal
8
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H Maeda
series ordinal
9
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S Minoshima
series ordinal
10
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language of work or name
English
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publication date
May 1995
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number of pages
2
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based on heuristic
inferred from page(s)
published in
Nature Genetics
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volume
10
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page(s)
9-10
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issue
1
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exact match
https://scigraph.springernature.com/pub.10.1038/ng0595-9
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cites work
Exon amplification: a strategy to isolate mammalian genes based on RNA splicing
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Drosophila single-minded gene encodes a nuclear protein with sequence similarity to the per gene product
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Drosophila single-minded gene encodes a helix-loop-helix protein that acts as a master regulator of CNS midline development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
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inferred from DOI database lookup
Molecular mapping of twenty-four features of Down syndrome on chromosome 21.
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human chromosome 21: genome mapping and exploration, circa 1993.
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
How many genes in the human genome?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
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inferred from DOI database lookup
Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycythemia in transgenic mice expressing the human erythropoietin gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Down syndrome phenotypes: the consequences of chromosomal imbalance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single-minded regulation of genes in the embryonic midline of the Drosophila central nervous system.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of a Factor Required for Activity of the Ah (Dioxin) Receptor
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of the Ah-receptor cDNA reveals a distinctive ligand-activated transcription factor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Continuum of overlapping clones spanning the entire human chromosome 21q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0595-9
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PubMed ID
7647800
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ResearchGate publication ID
15550956
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