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English
Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
title
Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
main subject
polydactyly
1 reference
based on heuristic
inferred from title
author name string
V Váradi
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
L Szabó
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
Z Papp
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
language of work or name
English
0 references
publication date
1 April 1980
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
volume
17
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
page(s)
119-122
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
cites work
Multiple congenital anomaly caused by an extra autosome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048515
retrieved
21 June 2018
Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048515
retrieved
21 June 2018
Genetic and clinical heterogeneity in the oral-facial-digital syndromes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048515
retrieved
21 June 2018
HOLOPROSENCEPHALY: A CASE REPORT WITH NO EXTRACRANIAL ABNORMALITIES AND NORMAL CHROMOSOME COUNT AND KARYOTYPE.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048515
retrieved
30 October 2018
Syndrome characterized by lingual malformation, Polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048515
retrieved
30 October 2018
Severe microphthalmus with Patau's syndrome (author's transl)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7381865
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.17.2.119
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
PMCID
1048515
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
PubMed ID
7381865
1 reference
stated in
Europe PubMed Central
PMCID
1048515
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7381865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
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