(Q57462560)

English

The syndrome of congenital telangiectaticerythema and stunted growth

scientific article

In more languages

default for all languages

No label defined

No description defined

edit

Statements

instance of

scholarly article

0 references

title

The syndrome of congenital telangiectatic erythema and stunted growth (English)

0 references

The syndrome of congenital telangiectaticerythema and stunted growth (English)

1 reference

stated in

Crossref

DOI

10.1016/S0022-3476(66)80426-2

reference URL

https://api.crossref.org/works/10.1016/S0022-3476(66)80426-2

11 July 2023

1 reference

Europe PubMed Central

PubMed publication ID

5901336

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5901336

retrieved

11 July 2023

author name string

D. Bloom

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5901336

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5901336

retrieved

11 July 2023

publication date

January 1966

0 references

language of work or name

English

0 references

full work available at URL

https://api.elsevier.com/content/article/PII:S0022347666804262?httpAccept=text/xml

1 reference

stated in

Crossref

DOI

10.1016/S0022-3476(66)80426-2

reference URL

https://api.crossref.org/works/10.1016/S0022-3476(66)80426-2

retrieved

11 July 2023

https://api.elsevier.com/content/article/PII:S0022347666804262?httpAccept=text/plain

1 reference

stated in

Crossref

DOI

10.1016/S0022-3476(66)80426-2

reference URL

https://api.crossref.org/works/10.1016/S0022-3476(66)80426-2

retrieved

11 July 2023

published in

The Journal of Pediatrics

0 references

volume

68

0 references

issue

1

0 references

page(s)

103-13

0 references

cites work

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980426-2

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Dwarfism with skin manifestations

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980426-2

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980426-2

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980426-2

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

POIKILODERMA CONGENITALE. REPORT OF TWO CASES

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980426-2

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Werner's syndrome; report of two cases

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980426-2

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Inheritance of an Abnormal Chromosome in Down's Syndrome (Mongolism) with Leukemia

series ordinal

11

1 reference

stated in

Crossref

DOI

10.1016/S0022-3476(66)80426-2

reference URL

https://api.crossref.org/works/10.1016/S0022-3476(66)80426-2

retrieved

11 July 2023

Non-endocrine dwarfism and pseudoepiphyses

series ordinal

23

1 reference

stated in

Crossref

DOI

10.1016/S0022-3476(66)80426-2

reference URL

https://api.crossref.org/works/10.1016/S0022-3476(66)80426-2

retrieved

11 July 2023

Identifiers

DOI

10.1016/S0022-3476(66)80426-2

0 references

PubMed publication ID

5901336

0 references

(Q57462560)

The syndrome of congenital telangiectaticerythema and stunted growth

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)