(Q28214855)

English

Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)

scientific article (publication date: June 2002)

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scholarly article

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Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome) (English)

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1 reference

based on heuristic

inferred from title

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author name string

M Faiyaz-Ul-Haque

1

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W Ahmad

2

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S H E Zaidi

3

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S Haque

4

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A S Teebi

5

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M Ahmad

6

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D H Cohn

7

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L-C Tsui

8

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language of work or name

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publication date

June 2002

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Clinical Genetics

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61

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6

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454-8

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Cellular interactions and signaling in cartilage development

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

The family of bone morphogenetic proteins

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

GDF5 coordinates bone and joint formation during digit development

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

Role of CDMP-1 in skeletal morphogenesis: promotion of mesenchymal cell recruitment and chondrocyte differentiation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

A human chondrodysplasia due to a mutation in a TGF-beta superfamily member

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

Mutations in CDMP1 cause autosomal dominant brachydactyly type C

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

Limb alterations in brachypodism mice due to mutations in a new member of the TGF beta-superfamily

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

21 January 2018

Fibular hypoplasia and complex brachydactyly (Du Pan syndrome) in an inbred Pakistani kindred

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

7 January 2021

based on heuristic

inferred from DOI database lookup

A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

7 January 2021

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inferred from DOI database lookup

Grebe syndrome: clinical and radiographic findings in affected individuals and heterozygous carriers

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Inductive activity of recombinant human growth and differentiation factor-5

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610610.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity alone

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1034/J.1399-0004.2002.610610.X

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10.1034/J.1399-0004.2002.610610.X

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