Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes
Author:
Publisher
Wiley
Subject
Developmental Biology
Reference40 articles.
1. Cerebellar Volume in Adults With Down Syndrome
2. Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse
3. Failed retrograde transport of NGF in a mouse model of Down's syndrome: Reversal of cholinergic neurodegenerative phenotypes following NGF infusion
4. An improved method for preparing G-banded chromosomes from mouse peripheral blood
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