(Q40117325)

17 September 2017

The Greig polysyndactyly-craniofacial dysmorphism syndrome (English)

1 reference

1 January 2023

main subject

multiple abnormalities

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A201464

1 January 2023

author name string

J. P. Fryns

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A201464

1 January 2023

W. Coeck

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A201464

1 January 2023

H. van den Berghe

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A201464

1 January 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=201464

1 January 2023

publication date

1 November 1977

1 reference

17 September 2017

4 November 1977

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=201464

full work available at URL

1 January 2023

http://link.springer.com/content/pdf/10.1007/BF00477055.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00477055/fulltext.html

1 January 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00477055

1 January 2023

1 reference

European Journal of Pediatrics

1 January 2023

published in

1 reference

17 September 2017

126

1 reference

17 September 2017

4

1 reference

17 September 2017

283-287

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00477055

17 September 2017

0 references

cites work

Acrocephalopolysyndactyly, type Noack, in a large kindred

1 reference

12 December 2020

Frontodigital syndrome: a dominantly inherited disorder with normal intelligence

1 reference

12 December 2020

Familial polysyndactyly and craniofacial anomalies.

1 reference

12 December 2020

Carpenter's syndrome: Acrocephalopolysyndactyly. An autosomal recessive syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00477055

1 reference

release_rofl3lplwbgbderujs7ldlnjcq

17 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rofl3lplwbgbderujs7ldlnjcq

24 November 2022

mapped directly with Wikidata item

1 reference