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English
Wither polygenic inheritance: mapping Hirschsprung disease
scientific article published on 01 August 1993
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
title
Wither polygenic inheritance: mapping Hirschsprung disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
author name string
Passarge E
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
publication date
1 August 1993
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
volume
4
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
page(s)
325-326
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0893-325
0 references
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A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
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Myenteric plexus in congenital megacolon; study of 11 cases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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FAMILIAL ABSENCE OF MYENTERIC PLEXUS (CONGENITAL MEGACOLON)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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Children of those treated surgically for Hirschsprung's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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Three-generation transmission of Hirschsprung's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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Association of Megacolon with Two Recessive Spotting Genes in the Mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Studies on megacolon in piebald mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of megacolon with a new dominant spotting gene (Dom) in the mouse
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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The association of Waardenburg syndrome and Hirschsprung megacolon
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: Possible variant of Waardenburg syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hirschsprung's Disease and Congenital Deafness
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hirschsprung's disease and congenital deafness. Familial assocation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple endocrine neoplasia type II B with symptoms suggesting Hirschsprung's disease: a case report
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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The origin of intrinsic ganglia of trunk viscera from vagal neural crest in the chick embryo
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular variant of angiotensinogen associated with preeclampsia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0893-325
retrieved
7 January 2021
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inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0893-325
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
PubMed ID
8401573
1 reference
stated in
Europe PubMed Central
PubMed ID
8401573
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401573%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
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