(Q40389756)

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A syndrome of osteogenesis imperfecta, optic atrophy, retinopathy and severe developmental delay in two sibs of consanguineous parents.

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Europe PubMed Central

PubMed publication ID

7515752

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

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title

A syndrome of osteogenesis imperfecta, optic atrophy, retinopathy and severe developmental delay in two sibs of consanguineous parents (English)

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stated in

Europe PubMed Central

PubMed publication ID

7515752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

main subject

osteogenesis imperfecta

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al Gazali LI

1

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Europe PubMed Central

PubMed publication ID

7515752

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

Sabrinathan K

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2

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Europe PubMed Central

PubMed publication ID

7515752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

Nair KG

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3

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Europe PubMed Central

PubMed publication ID

7515752

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

publication date

1 January 1994

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Europe PubMed Central

PubMed publication ID

7515752

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

published in

Clinical Dysmorphology

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Europe PubMed Central

PubMed publication ID

7515752

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

volume

3

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Europe PubMed Central

PubMed publication ID

7515752

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

issue

1

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Europe PubMed Central

PubMed publication ID

7515752

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

page(s)

55-62

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PubMed publication ID

7515752

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 October 2019

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PubMed publication ID

7515752

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7515752

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7515752%20AND%20SRC:MED&resulttype=core&format=json

(Q40389756)

A syndrome of osteogenesis imperfecta, optic atrophy, retinopathy and severe developmental delay in two sibs of consanguineous parents.

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