Genetic mapping of the dentinogenesis imperfecta type II locus.

Dentinogenesis imperfecta type II (DGI-II) is an autosomal dominant disorder of dentin formation, which has previously been mapped to chromosome 4q12-21. In the current study, six novel short tandem-repeat polymorphisms (STRPs) have been isolated, five of which show significant evidence of linkage t...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Crosby, A H, Scherpbier-Heddema, T, Wijmenga, C, Altherr, M R, Murray, J C, Buetow, K H, Dixon, M J
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1995
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801522/
https://ncbi.nlm.nih.gov/pubmed/7573043
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