(Q52497477)

English

Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement.

scientific article published in January 1974

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Statements

scholarly article

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement. (English)

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

author name string

T M Schroeder

1

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

J German

2

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

publication date

1 January 1974

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

25

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

299-306

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

4

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

[Spontaneous chromosomal instability in the rare hereditary diseases: Fanconi's anemia and Bloom's syndrome]

1 reference

https://api.crossref.org/works/10.1007%2FBF00336905

21 January 2018

[Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia].

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CYTOLOGICAL EVIDENCE FOR CROSSING-OVER IN VITRO IN HUMAN LYMPHOID CELLS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between chromosomal instability and leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Genetic factors in the development of cancer]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Course study of Fanconi's anemia in an adult

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonrandom distribution of chromosome breaks in Fanconi's anemia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

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/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The internal order of the interphase nucleus

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous chromosomal instability.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genes which increase chromosomal instability in somatic cells and predispose to cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4464237

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/4464237

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00336905

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/4464237

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