(Q48141938)

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A highly polymorphic (ACT)n VNTR (variable nucleotide of tandem repeats) locus inside intron 12 of COL1A2, one of the two genes involved in dominant osteogenesis imperfecta.

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/8104634

A highly polymorphic (ACT)n VNTR (variable nucleotide of tandem repeats) locus inside intron 12 of COL1A2, one of the two genes involved in dominant osteogenesis imperfecta. (English)

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/8104634

osteogenesis imperfecta

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Pepe G

1

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http://europepmc.org/abstract/MED/8104634

publication date

1 January 1993

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/8104634

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/8104634

2

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9 February 2018

http://europepmc.org/abstract/MED/8104634

300-305

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9 February 2018

http://europepmc.org/abstract/MED/8104634

4

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/8104634

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Conserved sequences and cell-specific DNase I hypersensitive sites upstream from the co-ordinately expressed alpha I- and alpha II-globin genes of Xenopus laevis.

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Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta

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Identifiers

10.1002/HUMU.1380020410

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/8104634

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/8104634

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