(Q38641263)

English

Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders

scientific article published on 23 October 2015

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Europe PubMed Central

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26589936

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5 September 2017

title

Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders (English)

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PubMed publication ID

5 September 2017

1

1 reference

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Europe PubMed Central

PubMed publication ID

26589936

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26589936%20AND%20SRC:MED&resulttype=core&format=json

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7 June 2020

Amy E Merrill

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2

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Europe PubMed Central

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26589936

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26589936%20AND%20SRC:MED&resulttype=core&format=json

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7 June 2020

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Cynthia L Neben

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1

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26589936

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5 September 2017

Amy E Merrill

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2

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Europe PubMed Central

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26589936

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5 September 2017

language of work or name

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23 October 2015

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5 September 2017

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Current Topics in Developmental Biology

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26589936

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26589936%20AND%20SRC:MED&resulttype=core&format=json

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7 June 2020

volume

115

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7 June 2020

page(s)

493-542

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26589936

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7 June 2020

cites work

Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/citations/10.1034/J.1399-0004.2002.610610.X

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DOI

10.1016/BS.CTDB.2015.09.005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

26589936

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26589936%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 June 2020

PubMed publication ID

26589936

1 reference

stated in

Europe PubMed Central

PubMed publication ID

26589936

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26589936%20AND%20SRC:MED&resulttype=core&format=json

(Q38641263)

Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders

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