(Q53760926)

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Preferential breakage of sensitive regions of human chromosomes.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

Preferential breakage of sensitive regions of human chromosomes. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

author name string

B R Reeves

1

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

S D Lawler

2

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

publication date

1 January 1970

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

8

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

4

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

295-301

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

Chromosome damage and polyploidization induced in human peripheral leukocytes in vivo and in vitro with nitrogen mustard, 6-mercaptopurine, and A-649

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective endoreduplication of the long arm of the 2 chromosome in a woman and her daughter

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomes and Transformation of Lymphocytes in Lymphoproliferative Disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The sites and relative frequencies of secondary constrictions in human somatic chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE SPECIFIC EFFECTS OF STREPTONIGRIN ACTIVITY ON HUMAN CHROMOSOMES IN CULTURE

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NON-RANDOM CHROMOSOMAL ABERRATIONS IN SV 40-TRANSFORMED HUMAN CELLS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two observations of identical breakages in the same group C chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The action of proflavin and actinomycin D in causing chromatid breakage in human cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome preparations of leukocytes cultured from human peripheral blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE EFFECT OF 5-BROMODEOXYURIDINE ON HUMAN CHROMOSOMES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous chromosome aberrations in familial panmyelopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

EFFECTS OF MITOMYCIN C ON HUMAN CHROMOSOMES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human small lymphocyte: its possible pluripotential quality

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Persisting clone of cells with an abnormal chromosome in a woman previously irradiated

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deleted chromosome 18 with paternal mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of a specific chromosome abnormality in leukocytes of a normal female

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/4245032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00280327

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 May 2018

http://europepmc.org/abstract/MED/4245032

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