(Q40494990)

21 September 2017

1 reference

title

The roles of collagen genes in skeletal development and morphogenesis (English)

1 reference

21 September 2017

1 reference

B. R. Olsen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7698270

31 August 2024

language of work or name

1 reference

1 March 1995

1 reference

21 September 2017

15 March 1995

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7698270

full work available at URL

31 August 2024

http://link.springer.com/content/pdf/10.1007/BF01931087.pdf

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1007/BF01931087

http://link.springer.com/article/10.1007/BF01931087/fulltext.html

31 August 2024

1 reference

https://api.crossref.org/works/10.1007/BF01931087

http://link.springer.com/content/pdf/10.1007/BF01931087

31 August 2024

1 reference

https://api.crossref.org/works/10.1007/BF01931087

31 August 2024

1 reference

21 September 2017

volume

51

1 reference

21 September 2017

issue

3

1 reference

21 September 2017

page(s)

194-195

1 reference

A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 gene

21 September 2017

cites work

1 reference

12 December 2020

Studies on cartilage. VI. A genetically determined defect in tracheal cartilage

1 reference

12 December 2020

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

1 reference

12 December 2020

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

1 reference

12 December 2020

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

1 reference

12 December 2020

A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesis

1 reference

12 December 2020

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01931087

1 reference

21 September 2017

1 reference