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X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28.

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Bibliografske podrobnosti
izdano v:J Med Genet
Main Authors: Fryns, J P, Spaepen, A, Cassiman, J J, van den Berghe, H
Format: Artigo
Jezik:Inglês
Izdano: BMJ Publishing Group 1991
Teme:
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016918/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1870106/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.28.6.429-a
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