(Q55846134)

English

Bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features: a newly recognized type of osteogenesis imperfecta

scientific article published on 01 January 1987

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

Bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features: a newly recognized type of osteogenesis imperfecta (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

craniosynostosis

0 references

osteogenesis imperfecta

0 references

1 reference

based on heuristic

inferred from title

author name string

D E Cole

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

T O Carpenter

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

language of work or name

0 references

publication date

1 January 1987

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

The Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

110

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

76-80

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

Genetic heterogeneity in osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980292-5

7 January 2021

Osteogenesis imperfecta: update and perspective

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980292-5

7 January 2021

Heritable diseases of collagen

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980292-5

7 January 2021

The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome.

2 references

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980292-5

7 January 2021

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980292-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Eye signs of hypophosphatasia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980292-5

7 January 2021

The syndrome of multisynostotic osteodysgenesis with long-bone fractures.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980292-5

7 January 2021

Identifiers

10.1016/S0022-3476(87)80292-5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3794889%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

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