(Q34464837)

2 August 2017

The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1. (English)

1 reference

camptodactyly-arthropathy-coxa vara-pericarditis syndrome

2 August 2017

0 references

author name string

Bahabri SA

1

1 reference

2 August 2017

Suwairi WM

2

1 reference

2 August 2017

Laxer RM

3

1 reference

2 August 2017

Polinkovsky A

4

1 reference

2 August 2017

Dalaan AA

5

1 reference

2 August 2017

Warman ML

6

1 reference

2 August 2017

1 April 1998

1 reference

2 August 2017

Arthritis & Rheumatology

1 reference

2 August 2017

41

1 reference

2 August 2017

4

1 reference

2 August 2017

730-735

1 reference

Pathologic features of a familial arthropathy associated with congenital flexion contractures of fingers

2 August 2017

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

Congenital contractural deformities of the fingers and arthropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

The camptodactyly-arthropathy-pericarditis syndrome: case report and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

Familial erosive arthritis associated with camptodactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

A truncated laminin chain homologous to the B2 chain: structure, spatial expression, and chromosomal assignment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

Characterization of the genomic structure, chromosomal location and promoter of human prostaglandin H synthase-2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1529-0131%28199804%2941%3A4%3C730%3A%3AAID-ART22%3E3.0.CO%3B2-Y

10.1002/1529-0131(199804)41:4<730::AID-ART22>3.0.CO;2-Y

21 January 2018

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DOI

1 reference

2 August 2017

1 reference