(Q39554199)

13 September 2017

1 reference

title

Osteogenesis imperfecta nosology and genetics (English)

1 reference

13 September 2017

osteogenesis imperfecta

0 references

author name string

Sillence DO

series ordinal

1

1 reference

PubMed ID

3063156

13 September 2017

language of work or name

English

0 references

publication date

1 January 1988

1 reference

Annals of the New York Academy of Sciences

13 September 2017

1 reference

13 September 2017

543

1 reference

13 September 2017

1-15

1 reference

Scanning electron microscopy of teeth in dominant osteogenesis imperfecta: support for genetic heterogeneity.

13 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55311.X

Valvular heart disease in osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55311.X

Osteogenesis imperfecta with unusual skeletal lesions: report of three families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55311.X

Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55311.X

International nosology of heritable disorders of connective tissue, Berlin, 1986

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55311.X

Subtle structural alterations in the chains of type I procollagen produce osteogenesis imperfecta type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55311.X

10.1111/J.1749-6632.1988.TB55311.X

21 January 2018

Identifiers

DOI

1 reference

13 September 2017

1 reference

PubMed ID

3063156