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Partial trisomy in a child with features suggesting mongolism
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
title
Partial trisomy in a child with features suggesting mongolism
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
author name string
H K Kumbnani
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
R A Pfeiffer
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
language of work or name
English
0 references
publication date
1 June 1969
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
volume
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
page(s)
201-205
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
cites work
Chromosome preparations of leukocytes cultured from human peripheral blood
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=1468861
retrieved
7 July 2018
[Reciprocal translocation between a chromosome number 21 (G1) and a chromosome of the group C(C6)]
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=1468861
retrieved
7 July 2018
Familial reciprocal translocation between a C group (12?) chromosome and a late labelling G chromosome.
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=1468861
retrieved
7 July 2018
Down's syndrome with unusual karyotype and thyroid autoantibodies
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=1468861
retrieved
7 July 2018
A case of G-G translocation in tandem
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/4240723
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A 1/G translocation in a member of a kindred with a marker chromosome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/4240723
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Down's syndrome associated with a familial (21q-; 22q+) translocation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/4240723
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A chromosomal abnormality in a girl with some features of Down's syndrome (mongolism)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/4240723
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
An unusual translocation in a case of Mongolism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/4240723
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
RECIPROCAL TRANSLOCATION AND MOSAICISM IN A MONGOL
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/4240723
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.6.2.201
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
PMC publication ID
1468861
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
PubMed publication ID
4240723
1 reference
stated in
Europe PubMed Central
PMC publication ID
1468861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240723%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
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