(Q39554215)

13 September 2017

1 reference

title

Osteogenesis imperfecta: the molecular basis of clinical heterogeneity (English)

1 reference

13 September 2017

osteogenesis imperfecta

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1 reference

Byers PH

1

1 reference

13 September 2017

Bonadio JF

2

1 reference

13 September 2017

Cohn DH

3

1 reference

13 September 2017

Starman BJ

4

1 reference

13 September 2017

Wenstrup RJ

5

1 reference

13 September 2017

Willing MC

6

1 reference

13 September 2017

language of work or name

English

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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

117-128

1 reference

Abnormal collagen metabolism in cultured cells in osteogenesis imperfecta

13 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55324.X

Reduced secretion of structurally abnormal type I procollagen in a form of osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55324.X

Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55324.X

Intron-mediated recombination may cause a deletion in an alpha 1 type I collagen chain in a lethal form of osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55324.X

Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55324.X

Lethal osteogenesis imperfecta resulting from a single nucleotide change in one human pro alpha 1(I) collagen allele

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55324.X

Type I osteogenesis imperfecta: a nonfunctional allele for pro alpha 1 (I) chains of type I procollagen

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55324.X

Nuclease S1 mapping of a homozygous mutation in the carboxyl-propeptide-coding region of the pro alpha 2(I) collagen gene in a patient with osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1988.TB55324.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.TB55324.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.TB55324.X

10.1111/J.1749-6632.1988.TB55324.X

21 January 2018

Identifiers

DOI

1 reference

13 September 2017

1 reference