(Q24681549)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5770175%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5770175%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

0 references

J. German

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5770175

27 June 2023

language of work or name

English

0 references

publication date

1 March 1969

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5770175%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

26 October 2019

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5770175/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5770175

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5770175/pdf/?tool=EBI

27 June 2023

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5770175

https://europepmc.org/articles/PMC1706430

27 June 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5770175

https://europepmc.org/articles/PMC1706430?pdf=render

27 June 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5770175

American Journal of Human Genetics

27 June 2023

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5770175%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

volume

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5770175%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

page(s)

196-227

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5770175%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5770175%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706430

Congenital telangiectatic erythema resembling lupus erythematosus in dwarfs; probably a syndrome entity.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706430

A simple method of estimating the segregation ratio under complete ascertainment

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706430

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706430

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706430

Genetic diseases, chromosome rearrangements, and malignancy.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706430

The syndrome of congenital telangiectaticerythema and stunted growth

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706430

Chromosome breakage and blastic transformation of lymphocytes in ataxia-telangiectasia

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706430

Chromosomal breakage and acute leukemia in congenital telangiectatic erythema and stunted growth

28 November 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Methodology in human genetics

1 reference

12 December 2020

1 reference

12 December 2020

Denouement and discussion. Bloom's syndrome. (Congenital telangiectasis erythema and stunted growth)

1 reference

12 December 2020

Biochemical defects in the blood cells in familial panmyelopathy (Fanconi type)

1 reference

12 December 2020

Congenital telangiectasic erythema with growth retardation (Bloom's syndrome)

1 reference

12 December 2020

A contribution to Bloom's syndrome. Congenital telangiectatic erythema resembling lypus erythematosus in dwarfs

1 reference

12 December 2020

Chromosal fragility in familial panmyelopathy (Fanconi type)

1 reference

12 December 2020

Eye findings in congenital telangiectatic erythema and growth retardation (Bloom's syndrome)

1 reference

12 December 2020

[Bloom syndrome. Case report with dermatohistological, endocrinologic, immunologic and cytogenetic studies]

1 reference

12 December 2020

Immunoglobulin Deficiency in Bloom's Syndrome

1 reference

12 December 2020

Birth weight and gestation time in relation to maternal age, parity and infant survival

1 reference

12 December 2020

Observations on the etiology of dwarfism in congenital telangiectatic erythema

1 reference

12 December 2020

Dwarfism with skin manifestations

1 reference

12 December 2020

Spontaneous chromosome aberrations in familial panmyelopathy

1 reference

12 December 2020

Bloom's syndrome. The syndrome of telangiectatic erythema and growth retardation

1 reference

12 December 2020

Hexokinase deficiency in blood cells in a group of kin with familial panmyelopathy (Fanconi type)

1 reference

12 December 2020

Chromosome Abnormalities in Constitutional Aplastic Anemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

3417803

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

3417803

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5770175%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

2 references

Consolidated OpenCitations Corpus – April 2017

3417803