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A homozygote for pericentric inversion of chromosome 4.
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1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
title
A homozygote for pericentric inversion of chromosome 4
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
author name string
N J Carpenter
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
B Say
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
N D Barber
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
language of work or name
English
0 references
publication date
1 December 1982
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
volume
19
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
issue
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
page(s)
469-471
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
cites work
Deletions of different segments of the long arm of chromosome 4.
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=1048967
retrieved
21 June 2018
Inherited pericentric inversion of chromosome no. 4.
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=1048967
retrieved
21 June 2018
Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3
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=1048967
retrieved
21 June 2018
Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)
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=1048967
retrieved
21 June 2018
Pericentric inversions of human chromosomes 9 and 10.
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=1048967
retrieved
21 June 2018
Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion.
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=1048967
retrieved
21 June 2018
Structural variation in chromosome No 9.
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=1048967
retrieved
21 June 2018
Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21)
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=1048967
retrieved
21 June 2018
Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4
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=1048967
retrieved
21 June 2018
Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18
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=1048967
retrieved
21 June 2018
The Wolf-Hirschhorn (4p-) 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=1048967
retrieved
21 June 2018
Inversion homozygosity of chromosome no. 9 in a higly inbred kindred
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=1048967
retrieved
21 June 2018
Pericentric inversions of chromosome 9 in two families
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6185681
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6185681
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6185681
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6185681
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Human Q and C chromosomal variations: distribution and incidence
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6185681
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6185681
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Proximal 4p-deletion: phenotype differs from classical 4p-syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6185681
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pericentric inversion and partial monosomy 4q associated with congenital anomalies
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6185681
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.19.6.469
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
PMC publication ID
1048967
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
PubMed publication ID
6185681
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048967
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
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