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Article

Osteogenesis imperfecta type VII maps to the short arm of chromosome 3

1 Jul 2002

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 12110407
DOI: 10.1016/s8756-3282(02)00808-6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Osteogenesis imperfecta type VII maps to the short arm of chromosome 3PMID 12110407Read ↗

Mapping of Autosomal Dominant Osteopetrosis Type II (Albers-Schönberg Disease) to Chromosome 16p13.3Semantic proximity Read ↗

Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.Semantic proximity Read ↗

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Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13Semantic proximity Read ↗

Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome.Semantic proximity Read ↗

Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28.Semantic proximity Read ↗

A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.Semantic proximity Read ↗

Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3.Semantic proximity Read ↗

A large interstitial deletion encompassing the amelogenin gene on the short arm of the Y chromosomeSemantic proximity Read ↗

A region on chromosome 3 is linked to dizygotic twinning.Semantic proximity Read ↗

Patient with novel interstitial deletion of chromosome 3q13.1q13.3 and agenesis of the corpus callosum.Semantic proximity Read ↗

[Bone malformations associated with deletion of the long arm of chromosome X].Semantic proximity Read ↗

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