(Q43629603)

English

Chromosome studies in 14 patients with disseminated sclerosis

scientific article published on January 1, 1971

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Chromosome studies in 14 patients with disseminated sclerosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

1 reference

10.1007/BF00446410

https://api.crossref.org/works/10.1007/BF00446410

20 December 2023

author name string

I. Emerit

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5115886

20 December 2023

R. Marteau

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5115886

20 December 2023

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 January 1971

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00446410.pdf

Portable Document Format

1 reference

10.1007/BF00446410

https://api.crossref.org/works/10.1007/BF00446410

20 December 2023

http://link.springer.com/article/10.1007/BF00446410/fulltext.html

1 reference

10.1007/BF00446410

https://api.crossref.org/works/10.1007/BF00446410

20 December 2023

http://link.springer.com/content/pdf/10.1007/BF00446410

1 reference

10.1007/BF00446410

https://api.crossref.org/works/10.1007/BF00446410

20 December 2023

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

13

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

25-33

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic studies in familial multiple sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MICROTECHNIC FOR THE STUDY OF HUMAN CHROMOSOMES FROM A HUMAN LEUKOCYTE CULTURE

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome anomalies in generalized scleroderma. A study of 6 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome Studies in Patients Treated With Azathioprine and Amethopterin

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

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/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[CYTOGENETIC STUDY OF 9 PATIENTS WITH MULTIPLE SCLEROSIS]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the condition of the chromosome complex in patients with disseminated sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autoimmunity and chromosomal aberrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effects of endoxan on HeLa cells chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/5115886

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00446410

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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