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English
Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly)
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
main subject
congenital disorder
0 references
hypertrichosis
1 reference
based on heuristic
inferred from title
Cantú syndrome
1 reference
based on heuristic
inferred from title
author
Rocío Sánchez-Urbina
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
María De Lourdes Ramirez-Dueñas
1 reference
stated in
ORCID Public Data File 2021
author name string
B Lazalde
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
I Nuño-Arana
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
W E Bitar
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
M de Lourdes Ramírez-Dueñas
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
publication date
1 October 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
volume
94
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
page(s)
421-427
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
cites work
A distinct osteochondrodysplasia with hypertrichosis- Individualization of a probable autosomal recessive entity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1096-8628%2820001023%2994%3A5%3C421%3A%3AAID-AJMG15%3E3.0.CO%3B2-9
retrieved
21 January 2018
An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1096-8628%2820001023%2994%3A5%3C421%3A%3AAID-AJMG15%3E3.0.CO%3B2-9
retrieved
21 January 2018
Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1096-8628%2820001023%2994%3A5%3C421%3A%3AAID-AJMG15%3E3.0.CO%3B2-9
retrieved
21 January 2018
Congenital hypertrichosis, cardiomegaly and mild osteochondrodysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1096-8628%2820001023%2994%3A5%3C421%3A%3AAID-AJMG15%3E3.0.CO%3B2-9
retrieved
21 January 2018
Identifiers
DOI
10.1002/1096-8628(20001023)94:5<421::AID-AJMG15>3.0.CO;2-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
PubMed publication ID
11050630
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11050630
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11050630%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
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