(Q28259445)

1

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I M Rasmussen

2

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J L Weber

3

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J Yuen

4

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K Reinker

5

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A P Garber

6

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D H Cohn

Length polymorphism within a complex dinucleotide repeat in the human decorin (DCN) gene

8

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language of work or name

English

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publication date

December 1993

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published in

Genomics

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volume

18

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issue

3

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page(s)

656-60

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Procollagen II Gene Mutation in Stickler Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Linkage of typical pseudoachondroplasia to chromosome 19

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

International classification of osteochondrodysplasias. International Working Group on Constitutional Diseases of Bone

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Identification of the molecular defect in a family with spondyloepiphyseal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

The mild form of pseudoachondroplasia. Identity of the morphological and biochemical alterations of growth cartilage with those of typical pseudoachondroplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

The biochemical defect of pseudoachondroplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Multiple epiphyseal dysplasia, Fairbank type: morphologic and biochemical study of cartilage

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 genes or DNA markers

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

A Mutation in the Amino-Terminal End of the Triple Helix of Type II Collagen Causing Severe Osteochondrodysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Exclusion of type II and type VI procollagen gene mutations in a five-generation family with multiple epiphyseal dysplasia.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

A second-generation linkage map of the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980369-6

7 January 2021

10.1016/S0888-7543(05)80369-6

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

8307576

1 reference

Consolidated OpenCitations Corpus – April 2017