(Q70683889)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

A case of pure red cell aplasia with a high incidence of spontaneous chromosome breakage: a possible X-ray sensitive syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

O Iskandar

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

M J Jager

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

R Willenze

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

A T Natarajan

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

publication date

1 January 1980

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

55

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

page(s)

337-340

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00290214

13 October 2019

exact match

0 references

cites work

Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). II. A discussion of the cytogenetic findings in Fanconi's anemia

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

Chromosome abnormality and hypocalcemia in congenital erythroid hypoplasia (blackfan-diamond syndrome)

1 reference

12 December 2020

Erythroid Precursors in Congenital Hypoplastic (Diamond-Blackfan) Anemia

1 reference

12 December 2020

Chromosomal radiosensitivity of ataxia telangiectasia cells at different cell cycle stages

1 reference

12 December 2020

In vitro chromosomal radiosensitivity in "chromosomal breakage syndromes"

1 reference

12 December 2020

Sensitivity to five mutagens in Fanconi's anemia as measured by the micronucleus method

1 reference

12 December 2020

Cytological detection of mutagen-carcinogen exposure by sister chromatid exchange

1 reference

12 December 2020

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

1 reference

12 December 2020

An improved method for the detection of micronuclei in human lymphocytes

1 reference

12 December 2020

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

1 reference

12 December 2020

The production of micronuclei from chromosome aberrations in irradiated cultures of human lymphocytes

1 reference

12 December 2020

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

1 reference

12 December 2020

In vitro chromosomal radiosensitivity in Fanconi's anemia

1 reference

12 December 2020

New Giemsa method for the differential staining of sister chromatids

1 reference

12 December 2020

Chromosome Abnormalities in Constitutional Aplastic Anemia

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00290214

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7203468%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference