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English
Nonrandom distribution of exchange points in patients with reciprocal translocations
scientific article published on 01 January 1980
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
title
Nonrandom distribution of exchange points in patients with reciprocal translocations
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
author name string
C Stoll
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%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
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%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
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
volume
56
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
page(s)
89-93
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
exact match
https://scigraph.springernature.com/pub.10.1007/bf00281575
0 references
cites work
[Chromatid exchanges in human mitotic cells. BUDR Treatment and bichromatic fluorescence by aridine orange (author's transl)]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
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De novo t(3 ; 20) (p 14 ; p 12) translocation in a young girl
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
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Radiation-induced non-random chromosome breakage
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
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Localization of γ-rays induced chromatid breaks using a three consecutive staining-technique
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
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Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
High resolution studies on the pattern of induced exchanges in the human karyotype
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
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Prenatal diagnosis and postnatal follow-up of an abnormal child with two de novo apparentely balanced translocations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Nonrandom distribution of exchange points in patients with structural rearrangements
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Balanced familial translocation t(5;19) (q12;p or q11) with phenotypical abnormalities in a girl
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Localization of sister chromatid exchanges in human chromosomes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
[Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Equilibrated 2-14 translocation in a mother and partial trisomy of a pair of the short branches of a number 2 chromosome in 2 of her children
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial 4q duplication due to inherited der(13),t(4;13)(q26;q34)mat in a girl with a deficiency of factor X.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
An analysis of the break points of structural rearrangements in man
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
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12 December 2020
based on heuristic
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Systematic analysis of 95 reciprocal translocations of autosomes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
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12 December 2020
based on heuristic
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Spontaneous repeated early abortions and familial t(5; 9) (p11; q33) translocation (author's transl)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
[Familial translocation t (16;19) (q24;q11) and birth of a girl with a trisomy 18]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Evidence for an inverse relationship between X-ray induced chromatid and chromosome breakage in human chromosomes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
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Identification withGandRBanding of the Position of Breakage Points Induced in Human Chromosomes byin VitroX-irradiation
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
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Inherited t2q-/15q+ translocation and Down's syndrome
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
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12 December 2020
based on heuristic
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An unusual partial trisomy 13
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
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12 December 2020
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Localization of chromatid breaks in Fanconi's anemia, using three consecutive stains
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7203485
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PubMed publication ID
7203485
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7203485
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203485%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
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