(Q35202474)

7 August 2017

The identification of fanconi anemia genotypes by clastogenic stress (English)

1 reference

7 August 2017

1 reference

M M Cohen

1

1 reference

7 August 2017

S J Simpson

2

1 reference

7 August 2017

G R Honig

3

1 reference

7 August 2017

H S Maurer

4

1 reference

7 August 2017

J W Nicklas

5

1 reference

7 August 2017

A O Martin

6

1 reference

7 August 2017

language of work or name

English

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publication date

1 September 1982

1 reference

American Journal of Human Genetics

7 August 2017

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7 August 2017

34

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7 August 2017

5

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7 August 2017

794-810

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Genetic heterogeneity of Fanconi's anemia demonstrated by somatic cell hybrids.

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

In vivo and in vitro chromosomal damage induced by LSD-25.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Nonrandom distribution of chromosome breaks in Fanconi's anemia.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Is Fanconi's anaemia defective in a process essential to the repair of DNA cross links?

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Formal genetics of Fanconi's anemia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Fanconi's Anemia With Growth Hormone Deficiency

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Inherited Aplastic Anaemia with Increased Endoreduplications: a New Syndrome or Fanconi's Anaemia Variant?

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Sv40 t-antigen expression in skin fibroblasts from clinically normal individuals and from ten cases of fanconi anemia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Genetic heterogeneity in xeroderma pigmentosum: complementation groups and their relationship to DNA repair rates

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Fanconi's anemia: the preanemic phase

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Effects of alkylating agents on lymphocytes from controls and from patients with Fanconi's anemia. Studies of sister chromatid exchanges, chromosome aberrations, and kinetics of cell division

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Unusual sensitivity of ataxia telangiectasia cells to bleomycin

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Mitomycin C test for diagnostic differentiation of idiopathic aplastic anemia and Fanconi anemia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685444

Chromosome Abnormalities in Constitutional Aplastic Anemia

26 September 2018

1 reference

12 December 2020

Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method

1 reference

12 December 2020

Spontaneous chromosome aberrations in familial panmyelopathy

1 reference

12 December 2020

Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects

1 reference

12 December 2020

Chromosomal peculiarities and ?in vitro? examinations in Fanconi's anaemia

1 reference

12 December 2020

Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease

1 reference

12 December 2020

Fanconi's Anaemia in the Genetics of Neoplasia

1 reference

12 December 2020

A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents

1 reference

12 December 2020

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

1 reference

12 December 2020

Chromosomal breaks in T and B lymphocytes in Fanconi's anemia

1 reference

12 December 2020

Clinical and cytogenetic observations during a six-year period in an adult with Fanconi's anaemia

1 reference

12 December 2020

Cross-link repair in human cells and its possible defect in Fanconi's anemia cells

1 reference

12 December 2020

Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells

1 reference

12 December 2020

Specific cellular defects in patients with Fanconi anemia

1 reference

12 December 2020

Mutagenic effects of isonicotinic acid hydracide in Fanconi's anemia

1 reference

12 December 2020

Specificity of bleomycin-induced cytotoxic effects on ataxia telangiectasia lymphoid cell lines

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

PMCID

1685444

1 reference

7 August 2017

1 reference