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Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.

A model is developed to account for recent molecular observations. It postulates four alleles: normal (N), small rather stable insert (S), larger, unstable insert (Z), and large insert (L). The last-named allele causes the fragile-X phenotype, inactivation of the FMR1 locus by methylation, and menta...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Morton, N E, Macpherson, J N
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1992
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC525664/
https://ncbi.nlm.nih.gov/pubmed/1570349
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