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Population studies of the fragile X: a molecular approach.

The fragile X mutation can now be recognised by a variety of molecular techniques. We report a pilot screening survey of a population of children with mental impairment in which we used Southern blotting methods to detect the fragile X mutation, augmented by cytogenetic studies on children whose phe...

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Bibliografski detalji
Izdano u:J Med Genet
Glavni autori: Jacobs, P A, Bullman, H, Macpherson, J, Youings, S, Rooney, V, Watson, A, Dennis, N R
Format: Artigo
Jezik:Inglês
Izdano: BMJ Publishing Group 1993
Teme:
Online pristup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016415/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8326487/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.6.454
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