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The 11q;22q translocation: a European collaborative analysis of 43 cases
scientific article published on 01 January 1980
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
title
The 11q;22q translocation: a European collaborative analysis of 43 cases
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
author
Charles Edmund Ford
series ordinal
3
object named as
C E Ford
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
author name string
M Fraccaro
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
J Lindsten
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
L Iselius
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
publication date
1 January 1980
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
published in
Human Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
volume
56
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
page(s)
21-51
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
cites work
The problem of partial trisomy 22 reconsidered
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Abnormal chromosome 22 and recurrence of trisomy-22 syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Balanced translocation, impaired sperm motility, and offspring anomaly
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Trisomy 11q. Individualization of a new syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cat eye syndrome. Partial trisomy 22 due to translocation in the mother
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Transposition of 9q34 and 22 (q11?qter) regions has a specific role in chronic myelocytic leukemia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A case of chronic myelogenous leukemia (CML) with a translocation between chromosomes 12 and 22, t(12;22) (p13;q13), resulting in a Philadelphia (Ph<sup>1</sup>) chromosome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A deleted extra chromosome 22 identified by DNA replication banding
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Evidence that chromosome band 22q12 is concerned with cell proliferation in chronic myeloid leukaemia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial trisomy of 11 and 22 due to familial translocation t(11;22) (q23;q11), inherited in three generations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
MONGOLISM AND OTHER ABNORMALITIES IN A FAMILY WITH TRISOMY 21-22 TENDENCY
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
2 cases of trisomy 11q(q23.2-- qter) with the same abnormality of external genitalia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Trisomy 22q-
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Deletion of the long arm of chromosome 11: a clinical entity
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial trisomy of the long arm of the chromosme 11 by malsegregation of a maternal translocation t(11;22)(q23 1;q1 11)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial monosomy due to long-arm deletion of chromosome 11 : del (11) (q23) (author's transl)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203479
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/BF00281567
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
PubMed publication ID
7203479
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203479
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203479%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
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